Colorectal Cancer, Hereditary Nonpolyposis, Type 2; Hnpcc2

Clinical Features

Top most frequent phenotypes and symptoms related to Colorectal Cancer, Hereditary Nonpolyposis, Type 2; Hnpcc2

  • Seizures
  • Muscular hypotonia
  • Flexion contracture
  • Neoplasm
  • Visual impairment
  • Dysarthria
  • Gait disturbance
  • Hypertonia
  • Coma
  • Behavioral abnormality
And another 48 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Colorectal Cancer, Hereditary Nonpolyposis, Type 2; Hnpcc2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Macrocephaly.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

PIK3CA, GLI3, EZH2, NFIX, UPF3B, MED12, CUL4B, PHF6, PTCH1, NSD1, PTEN
Specificity
10 %
Genes
10 %
Somatic Overgrowth Gene Panel.

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine in United States.

AKT1, AKT3, PIK3R2, GNA11, GNAQ, AKT2, PIK3CA, MTOR
Specificity
13 %
Genes
10 %
PIK3CA.

By Institute for Human Genetics University Clinic Freiburg in Germany.

PIK3CA
Specificity
100 %
Genes
10 %
Vascular Malformations NGS Multi-Gene Panel (21 Genes).

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

ANTXR1, DOCK6, MAP3K3, KDR, GNAQ, PIK3CA, TEK, GLMN, BMPR2, CAV1, KCNK3, GDF2, ACVRL1, SOX18, RASA1, PDCD10, CCM2, KRIT1, ENG, SMAD4 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Megalencephaly-polymicrogyria and dysplastic megalencephaly (NGS panel of 8 genes).

By CGC Genetics in Portugal.

NPRL3, CCND2, AKT3, PIK3R2, PIK3CA, EZH2, MTOR, DEPDC5
Specificity
13 %
Genes
10 %
Mental retardation - different panels.

By Institute of Human Genetics Cologne University in Germany.

EEF1B2, UBR7, PARP1, CAPN10, SLC31A1, TRMT1, PGAP2, GMPPA, TANGO2, IMPA1, RALGDS, ZBTB40, KCNK9, SETD1A, HERC2, TM4SF20, AHDC1, CCDC88A, ACBD6, KDM5A , (...)

View the complete list with 847 more genes
Specificity
1 %
Genes
28 %
Hereditary kidney disorders - different panels.

By Institute of Human Genetics Cologne University in Germany.

CLDN10, TMEM260, KANK3, SLC6A20, MAGEC1, TBC1D1, SLC41A1, SLC36A2, SLC22A10, KCNMB1, NRIP1, MAGED2, DYNC2LI1, IFT52, RMND1, MAPKBP1, MOCOS, SLC26A1, PDE3A, FN1 , (...)

View the complete list with 391 more genes
Specificity
1 %
Genes
19 %
Macrocephaly.

By MGZ Medical Genetics Center in Germany.

DIS3L2, CCND2, HEPACAM, TBC1D7, KPTN, AKT1, AKT3, PIK3R2, GNAQ, PIK3CA, KIF7, GPSM2, GLI3, RNF135, EZH2, NFIX, DNMT3A, ABCC6, BRWD3, UPF3B , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
10 %
Mental Retardation and Dysmorphology - panels.

By MGZ Medical Genetics Center in Germany.

GATAD2B, CUL7, SPECC1L, IRF6, CCNQ, ROR2, CCND2, HEPACAM, TBC1D7, KPTN, WNT5A, SRCAP, UBR1, C2CD3, TCTN3, NOTCH2, PACS1, EPG5, ERCC8, AKT1 , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
19 %
Syndromal Diseases - panels.

By MGZ Medical Genetics Center in Germany.

PACS1, EPG5, ERCC8, AKT1, AKT3, PIK3R2, INSR, IDH1, ALX1, GNAQ, PIK3CA, CPLANE1, KIF7, GNAS, TRIM37, EFTUD2, EFNB1, EP300, TBX5, SALL4 , (...)

View the complete list with 322 more genes
Specificity
1 %
Genes
19 %
Brain Malformations / Neuronal Migration Disorders.

By MGZ Medical Genetics Center in Germany.

NXF5, HERC2, ARHGEF15, JAM3, DARS, CLP1, DIS3L2, COL4A2, POLR3B, POLR3A, ITM2B, STUB1, NOL3, SEPSECS, KCNH5, ZNF674, KIF2A, KIF5C, TUBB, TUBG1 , (...)

View the complete list with 246 more genes
Specificity
1 %
Genes
10 %
Cancer Hotspot Panel.

By Centogene AG - the Rare Disease Company in Germany.

MYCL, ROS1, RPTOR, KIF5B, GNAI2, GNA13, EML4, BRD4, ARAF, NFE2L2, GNG2, KEAP1, NRG1, CCNE1, CD74, RICTOR, ERBB4, MYC, BCL6, SMO , (...)

View the complete list with 68 more genes
Specificity
4 %
Genes
28 %
CLOVE syndrome.

By Centogene AG - the Rare Disease Company in Germany.

PIK3CA
Specificity
100 %
Genes
10 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

FCGR2B, TNF, ALOX5AP, PRKCH, TLR5, TIRAP, NOS2, XBP1, KCNK18, AANAT, SNIP1, EIF4E, ZBTB18, ADAM10, YAP1, ICAM1, SNX3, CISH, TAS2R38, FRG1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
28 %
Neuronal Migration Disorders Panel.

By CeGaT GmbH in Germany.

DCHS1, SNAP29, KIF2A, KIF5C, TUBG1, RTTN, PIK3R2, VLDLR, IER3IP1, RAB18, PIK3CA, EOMES, RAB3GAP2, GMPPB, POMK, FAT4, LAMC3, MED12, ACTG1, ACTB , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
10 %
RASopathies Panel.

By CeGaT GmbH in Germany.

CCND2, AKT3, PIK3R2, PIK3CA, STAMBP, A2ML1, RRAS, RASA2, SPRED1, RASA1, NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
19 %
Neuronal Migration Disorders Panel.

By CeGaT GmbH in Germany.

DCHS1, SNAP29, KIF2A, KIF5C, TUBG1, RTTN, PIK3R2, VLDLR, IER3IP1, RAB18, PIK3CA, EOMES, RAB3GAP2, GMPPB, POMK, FAT4, LAMC3, MED12, ACTG1, ACTB , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
10 %
Macrocephaly Panel.

By CeGaT GmbH in Germany.

HEPACAM, AKT3, PIK3R2, DHCR24, PIK3CA, EZH2, NFIX, MED12, GFAP, PIGN, PIGA, MLC1, GPC3, NSD1, ASPA, GCDH, PTEN
Specificity
6 %
Genes
10 %
RASopathies Panel.

By CeGaT GmbH in Germany.

CCND2, AKT3, PIK3R2, PIK3CA, STAMBP, A2ML1, RRAS, RASA2, SPRED1, RASA1, NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
19 %
PIK3CA-Related Segmental Overgrowth (Cowden Syndrome 5): PIK3CA gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PIK3CA
Specificity
100 %
Genes
10 %
Melanoma: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

WRN, GNAQ, PIK3CA, BAP1, KIT, CDKN2A, CDK4, NRAS, MAP2K1, KRAS, BRAF, RB1, PTEN
Specificity
16 %
Genes
19 %
Neuronal Migration Disorder Panel.

By Blueprint Genetics in Finland.

YWHAE, COL4A2, SEPSECS, LAMB1, MPDZ, TUBG1, KATNB1, RTTN, OCLN, AKT3, PIK3R2, VLDLR, RAB18, PIK3CA, KIF7, RAB3GAP2, GMPPB, GPSM2, FLVCR2, TUBB2A , (...)

View the complete list with 38 more genes
Specificity
2 %
Genes
10 %
Comprehensive Skeletal Dysplasias and Disorders Panel.

By Blueprint Genetics in Finland.

CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, BHLHA9, WDR34, FAM83H , (...)

View the complete list with 226 more genes
Specificity
1 %
Genes
19 %
Lymphatic Malformations and Related Disorders Panel.

By Blueprint Genetics in Finland.

PIK3CA, FLT4, KIF11, CCBE1, SOX18, RASA1, FAT4, PIEZO1, FOXC2, GATA2, GJC2
Specificity
10 %
Genes
10 %
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel.

By Blueprint Genetics in Finland.

IRS1, CKAP2L, LONP1, NANS, EXTL3, DLL4, TBX4, KIF22, ADAMTS17, ACAN, PAPSS2, NOG, ENAM, TBX6, DVL1, LTBP3, XYLT1, IHH, IGFALS, BHLHA9 , (...)

View the complete list with 288 more genes
Specificity
1 %
Genes
28 %
Focus::Oncomine™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

JAK1, ESR1, ROS1, ERBB4, SMO, ERBB2, DDR2, AKT1, GNA11, IDH1, PDGFRA, JAK2, EGFR, GNAQ, PIK3CA, JAK3, KIT, ERBB3, MTOR, CTNNB1 , (...)

View the complete list with 15 more genes
Specificity
6 %
Genes
19 %
Focus::Renal® NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

RHEB, HIF1A, PBRM1, EPHB4, ROS1, AXL, SMO, ERBB2, PDGFRB, AKT1, ABL1, EGFR, FLT3, AKT2, PIK3CA, BAP1, KIT, ARID1A, MTOR, KDM5C , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
10 %
Somatic Overgrowth Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

SMO, AKT1, AKT3, PIK3R2, GNA11, IDH1, GNAQ, AKT2, PIK3CA, MTOR, RASA1, TSC1, TSC2, IDH2, PTEN
Specificity
7 %
Genes
10 %
Solid Tumor Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

BCL2L1, H3F3A, KLF4, TRAF7, PIK3C2B, HIST1H3B, JAK1, MCL1, PBRM1, DAXX, CDKN1A, MYB, MYBL1, RAD54B, ESR2, ESR1, KMT2C, FGFR4, ROS1, NFE2L2 , (...)

View the complete list with 102 more genes
Specificity
4 %
Genes
37 %
Head & Neck Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

RHOA, BCL2L1, PIK3C2B, MCL1, KMT2C, NFE2L2, RAC1, FAT1, AFF3, ERBB2, CCND1, NOTCH2, PIK3R1, AKT1, AKT3, FBXW7, EGFR, AKT2, PIK3CA, GATA4 , (...)

View the complete list with 21 more genes
Specificity
8 %
Genes
28 %
FoundationOne® Heme.

By Foundation Medicine, Inc. in United States.

TRAF5, PIM1, PRDM1, HIST1H2AG, HIST1H3B, HIST1H1C, HDAC1, GTSE1, HIST1H1D, HIST1H2BK, HIST1H2BO, HIST1H2BC, HIST1H2AC, HIST1H2AM, HIST1H1E, HIST1H2AL, HDAC7, HIST1H2BJ, INPP5D, IKZF2 , (...)

View the complete list with 385 more genes
Specificity
2 %
Genes
55 %
Cancer Hotspot Analysis.

By Advanced Technology Laboratory Spectrum Health in United States.

ERBB4, SMO, ERBB2, KDR, SRC, AKT1, GNA11, FBXW7, IDH1, PDGFRA, ABL1, JAK2, EGFR, NPM1, FLT3, GNAQ, CSF1R, PIK3CA, GNAS, JAK3 , (...)

View the complete list with 30 more genes
Specificity
6 %
Genes
28 %
Circulo Colorectal.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Circulo Lung.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Circulo Melanoma.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Circulo Gastric.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Hereditary Cancer Comprehensive Panel.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

TP53BP1, KLLN, CHEK1, GEN1, MYH15, MYH1, MYH13, MYH4, PPM1D, HOXB13, MYH10, GALNT12, RAD51, AKT1, POLE, ABRAXAS1, ETV6, GREM1, POLD1, PIK3CA , (...)

View the complete list with 53 more genes
Specificity
9 %
Genes
55 %
NeoTYPE® Discovery Profile for Solid Tumors.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

IKBKE, INPP4B, HSP90AA1, LRP1B, BCL2L2, AURKB, LMO1, ARFRP1, MDM4, MAP2K4, MCL1, EMSY, CHEK1, PBRM1, DAXX, PDCD1LG2, EPHB1, EPHA3, DOT1L, EPHA5 , (...)

View the complete list with 295 more genes
Specificity
3 %
Genes
64 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

ETV1, BCL3, SET, ELL, BTG1, ADGRA2, ACSL3, AFF1, ACSL6, ACKR3, RABEP1, PSIP1, RANBP17, RAD51B, RPL22, SDC4, SH3GL1, REL, SLC45A3, SYK , (...)

View the complete list with 571 more genes
Specificity
2 %
Genes
73 %
OmniSeq Comprehensive.

By OmniSeq, Inc. in United States.

NKX2-8, RHOA, BCL2L1, ETV4, ETV1, GAS6, RPS6KB1, RHEB, SPOP, TIAF1, XPO1, ZNF217, JAK1, KNSTRN, IFITM1, APEX1, ATP11B, MDM4, BCL9, BIRC2 , (...)

View the complete list with 124 more genes
Specificity
3 %
Genes
37 %
Cowden Syndrome, Sequencing PIK3CA Gene.

By Reference Laboratory Genetics in Spain.

PIK3CA
Specificity
100 %
Genes
10 %
Megalencephaly-Capillary Malformation-Polymicrogyria Syndrome , Sequencing PIK3CA Gene.

By Reference Laboratory Genetics in Spain.

PIK3CA
Specificity
100 %
Genes
10 %
Macrocephaly , Panel Massive Sequencing (NGS) 16 Genes.

By Reference Laboratory Genetics in Spain.

HEPACAM, AKT3, PIK3R2, DHCR24, PIK3CA, EZH2, NFIX, MED12, GFAP, PIGN, PIGA, MLC1, GPC3, NSD1, ASPA, PTEN
Specificity
7 %
Genes
10 %
Malformations of Cortical Development , Panel Massive Sequencing (NGS) 38 Genes.

By Reference Laboratory Genetics in Spain.

LAMB1, OCLN, AKT3, PIK3R2, VLDLR, PIK3CA, GPSM2, LAMC3, ACTG1, ACTB, CASK, OPHN1, KIF1BP, TUBB2B, SRPX2, ADGRG1, PAFAH1B1, FLNA, TUBA8, RELN , (...)

View the complete list with 18 more genes
Specificity
3 %
Genes
10 %
Glioma (Susceptibility to Somatic) , Panel Massive Sequencing (NGS) 12 Genes.

By Reference Laboratory Genetics in Spain.

ERBB2, IDH1, EGFR, PIK3CA, LGI1, BRAF, PRKN, IDH2, RB1, TP53, PTEN, BRCA2
Specificity
9 %
Genes
10 %
152 Integrated Advantage NGS Solid Tumor Panel.

By Integrated Molecular Diagnostics Pathology, Inc. in United States.

AURKA, TOP1, ABCC1, SLC29A1, STK11IP, SYK, SULT1A1, XRCC1, TOP2A, TOP2B, PLK1, JAK1, JUN, IKBKE, BCL2L2, AURKB, MDM4, MAP2K4, EMSY, CHEK1 , (...)

View the complete list with 132 more genes
Specificity
3 %
Genes
37 %
Tempus xT assay.

By Tempus Labs, Inc. in United States.

HLA-DRB5, HLA-C, PPP6C, ZNRF3, FOXQ1, TBC1D12, WEE1, YEATS4, POU2F2, C8orf34, SEMA3C, PDPK1, HLA-G, LAG3, CCDC6, MEF2B, AURKA, TOP1, P2RY8, FGF4 , (...)

View the complete list with 571 more genes
Specificity
2 %
Genes
91 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

SETD6, PIM3, MAP3K10, PDGFA, MAP3K11, PAK2, KHSRP, WASL, CASC11, GLIS1, NRG2, SOX21, SMARCC1, CUL4A, UTY, WNT9A, TEF, CHIC1, TRIM28, CDK11B , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
91 %
CEN4GEN Comprehensive Hereditary Cancer Syndrome: Gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

RAD51B, EHBP1, POU6F2, EPHB2, MSMB, ASCC1, MSR1, XRCC3, PTCH2, PALLD, MLH3, DDB2, DIS3L2, MTAP, POLH, UROD, TMC8, TMC6, PDE11A, XPC , (...)

View the complete list with 123 more genes
Specificity
5 %
Genes
64 %
CEN4GEN Gastric cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

WNK2, ADGRB3, SSTR1, TRRAP, LRP1B, LPAR2, GPR78, ATP4A, CCNE1, TRIO, DCC, MYC, ERBB2, PRKDC, FBXW7, PIK3CA, SPEG, NOTCH1, CTNNB1, S1PR2 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
CEN4GEN Lung cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

ADGRB3, LRP1B, EPHA5, MUC16, GRM8, PIK3CG, ROS1, NFE2L2, KEAP1, ERBB4, MYC, ERBB2, MDM2, RUNX1T1, AKT1, FBXW7, PDGFRA, EGFR, RARB, PIK3CA , (...)

View the complete list with 24 more genes
Specificity
7 %
Genes
28 %
CEN4GEN Prostate cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SPOP, ZNF473, THSD7B, ZNF595, KDM4B, NRCAM, OR5L1, PDZRN3, NKX3-1, NIPA2, KLF6, GLI1, MYC, CDK12, SCN11A, TBX20, PIK3CA, CDKN1B, AKAP9, MED12 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
10 %
CEN4GEN Comprehensive targeted oncogene tumor mutation screen (somatic genetic testing): Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

ERBB4, SMO, ERBB2, KDR, SRC, AKT1, GNA11, FBXW7, IDH1, PDGFRA, ABL1, JAK2, EGFR, NPM1, FLT3, GNAQ, CSF1R, PIK3CA, GNAS, JAK3 , (...)

View the complete list with 28 more genes
Specificity
7 %
Genes
28 %
Comprehensive Brain Malformation Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

DISP1, VLDLR, MYCN, RBBP8, IER3IP1, RAB18, PIK3CA, GAS1, EOMES, DLL1, ARL13B, CPLANE1, CEP41, KIF7, RPGRIP1L, TCTN1, TCTN2, TMEM138, TMEM237, TTC21B , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
10 %
PIK3CA sequence analysis (Somatic).

By Genetic Diagnostic Laboratory University of Pennsylvania School of Medicine in United States.

PIK3CA
Specificity
100 %
Genes
10 %
PIK3CA Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Hereditary Thyroid Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

DICER1, SRGAP1, WRN, AKT1, PIK3CA, PRKAR1A, CHEK2, SDHD, SDHB, RET, TP53, PTEN, APC
Specificity
8 %
Genes
10 %
Segmental Overgrowth Disorders - NGS panel (8 genes).

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

AKT1, AKT3, PIK3R2, PIK3CA, MTOR, TSC1, TSC2, PTEN
Specificity
13 %
Genes
10 %
PIK3CA. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PIK3CA
Specificity
100 %
Genes
10 %
Macrocephaly (NGS panel for 16 genes).

By CGC Genetics in Portugal.

HEPACAM, AKT3, PIK3R2, DHCR24, PIK3CA, EZH2, NFIX, MED12, GFAP, PIGN, PIGA, MLC1, GPC3, NSD1, ASPA, PTEN
Specificity
7 %
Genes
10 %
Cowden syndrome type 5 (sequence analysis of PIK3CA gene).

By CGC Genetics in Portugal.

PIK3CA
Specificity
100 %
Genes
10 %
Megalencephaly-polymicrogyria and dysplastic megalencephaly (NGS panel of 8 genes).

By CGC Genetics in Portugal.

NPRL3, CCND2, AKT3, PIK3R2, PIK3CA, EZH2, MTOR, DEPDC5
Specificity
13 %
Genes
10 %
Cowden syndrome type 5 (sequence analysis of PIK3CA gene).

By CGC Genetics in Portugal.

PIK3CA
Specificity
100 %
Genes
10 %
Cowden and Cowden-like Syndromes via the PIK3CA Gene.

By PreventionGenetics PreventionGenetics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Colorectal adenocarcinoma, somatic mutation sequencing panel.

By Molecular Diagnostics Laboratory University Health Network in Canada.

PIK3CA, NRAS, KRAS, BRAF
Specificity
50 %
Genes
19 %
Custom solid tumor gene sequencing panel.

By Molecular Diagnostics Laboratory University Health Network in Canada.

RAC1, RICTOR, EIF1AX, HOXD8, ERBB4, CDKN2B, ERBB2, DDB2, CCND1, XPC, KDR, ERCC5, PDGFRB, CDK6, AKT1, GNA11, PDGFRA, SF3B1, EGFR, GNAQ , (...)

View the complete list with 25 more genes
Specificity
5 %
Genes
19 %
Megalencephaly.

By MGZ Medical Genetics Center in Germany.

CCND2, AKT1, AKT3, PIK3R2, PIK3CA, TSC1, TSC2, PTEN
Specificity
13 %
Genes
10 %
Solid Tumor Panel.

By Centogene AG - the Rare Disease Company in Germany.

KMT2C, FGFR4, NTRK3, ROS1, AXL, SMO, ERBB2, DDR2, KDR, PDGFRB, PIK3R1, AKT1, GNA11, IDH1, PDGFRA, ABL1, JAK2, EGFR, GNAQ, PIK3CA , (...)

View the complete list with 42 more genes
Specificity
5 %
Genes
28 %
Disorders associated with malignancy Panel.

By CeGaT GmbH in Germany.

DDB2, POLH, XPC, RHBDF2, GTF2H5, CYLD, XPA, ERCC5, PDGFRB, FERMT1, ERCC8, AKT1, AXIN2, PIK3CA, ERCC4, NOP10, NHP2, WRAP53, CTC1, ERCC6 , (...)

View the complete list with 25 more genes
Specificity
12 %
Genes
46 %
Familial Tumor Syndromes Panel.

By CeGaT GmbH in Germany.

RASAL1, CYLD, DICER1, WRN, AKT1, PIK3CA, BAP1, SMARCB1, SMARCA4, SMARCE1, ATR, SPRED1, LZTR1, NF1, CDC73, MET, SDHD, CDKN2A, NF2, NBN , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
10 %
Macrocephaly Panel.

By CeGaT GmbH in Germany.

HEPACAM, AKT3, PIK3R2, DHCR24, PIK3CA, EZH2, NFIX, MED12, GFAP, PIGN, PIGA, MLC1, GPC3, NSD1, ASPA, GCDH, PTEN
Specificity
6 %
Genes
10 %
RASopathies Panel.

By CeGaT GmbH in Germany.

CCND2, AKT3, PIK3R2, PIK3CA, STAMBP, A2ML1, RRAS, RASA2, SPRED1, RASA1, NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 3 more genes
Specificity
9 %
Genes
19 %
CLOVE syndrome, somatic (PIK3CA).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

PIK3CA
Specificity
100 %
Genes
10 %
NOONAN, LEOPARD, COSTELLO and CARDIOFACIOCUTANEOUS SYNDROME.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PRKCB, PIK3CG, LRP1, CRKL, PIK3CB, MAPK1, GAB2, CRK, SPRY2, IL2, PRKCH, RAC1, ERBB2, SRC, IL2RA, SRCAP, PIK3R1, PIK3CD, AKT1, PIK3R2 , (...)

View the complete list with 24 more genes
Specificity
5 %
Genes
19 %
PIK3CA.

By Fulgent Genetics Fulgent Genetics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Hemato-oncology chromosomal microarray.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

NUTM2B, NUTM2A, SSX2, MALAT1, ETV4, TFEB, SSX4, NR4A3, MSI2, CREB3L2, TFE3, FOXO1, ETV1, ACSL3, RABEP1, SSX1, SS18, POU5F1, HEY1, JUN , (...)

View the complete list with 72 more genes
Specificity
4 %
Genes
28 %
Macrocephaly / Overgrowth Syndrome Panel.

By Blueprint Genetics in Finland.

EED, DIS3L2, MPDZ, CCND2, HEPACAM, KPTN, AKT1, AKT3, PIK3R2, DHCR24, PIK3CA, KIF7, GPSM2, GLI3, RNF135, EZH2, NFIX, DNMT3A, BRWD3, UPF3B , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
10 %
Vascular Malformations Panel.

By Blueprint Genetics in Finland.

ELMO2, PIK3CA, TEK, STAMBP, GLMN, ACVRL1, SOX18, RASA1, PDCD10, CCM2, KRIT1, ENG, SMAD4, PTEN
Specificity
8 %
Genes
10 %
PIK3CA Mutation by Sequencing.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Liquid::Lung-cfDNA™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

ROS1, ERBB2, EGFR, PIK3CA, MET, ALK, NRAS, MAP2K1, KRAS, BRAF, TP53
Specificity
19 %
Genes
19 %
PIK3CA-Related Overgrowth Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Nevus Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

GNA11, GNAQ, PIK3CA, NRAS, KRAS, HRAS, FGFR3
Specificity
29 %
Genes
19 %
CNS Tumor Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

H3F3A, KLF4, TRAF7, HIST1H3B, DAXX, FUBP1, MYB, MYBL1, CIC, MYC, SMO, MN1, ERBB2, NTRK2, PIK3R1, AKT1, IDH1, PDGFRA, EGFR, PIK3CA , (...)

View the complete list with 28 more genes
Specificity
5 %
Genes
19 %
Melanoma Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

KMT2C, ROS1, RAC1, ERBB4, ERBB2, CCND1, PDGFRB, AKT1, GNA11, PDGFRA, EGFR, GNAQ, PIK3CA, BAP1, KIT, TERT, MTOR, CTNNB1, MED12, KMT2D , (...)

View the complete list with 18 more genes
Specificity
6 %
Genes
19 %
Breast Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

RAD54B, ESR2, ESR1, RAC1, ERBB4, ERBB2, KDR, CDK6, PIK3R1, AKT1, FBXW7, IDH1, EGFR, PIK3CA, FANCA, KIT, ERBB3, GATA3, FGFR1, BRIP1 , (...)

View the complete list with 22 more genes
Specificity
5 %
Genes
19 %
Genitourinary Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

PBRM1, CDKN1A, KMT2C, RXRA, ERBB2, PIK3R1, AKT1, AKT3, FBXW7, STAG2, EGFR, AKT2, PIK3CA, BAP1, ERBB3, TERT, KDM6A, MTOR, MED12, ERCC2 , (...)

View the complete list with 24 more genes
Specificity
5 %
Genes
19 %
Gynecologic Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

ERBB4, PPP2R1A, FAT1, SMO, ERBB2, CDK12, CCND1, KDR, PIK3R1, AKT1, AKT3, PIK3R2, POLE, FBXW7, ABL1, EGFR, AKT2, POLD1, PIK3CA, JAK3 , (...)

View the complete list with 30 more genes
Specificity
6 %
Genes
28 %
Cowden Syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

AKT1, PIK3CA, SDHD, SDHB, PTEN
Specificity
20 %
Genes
10 %
PIK3CA Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Guardant360.

By Guardant Health in United States.

MAPK3, RHOA, RHEB, MAPK1, ESR1, NTRK3, ROS1, ARAF, NFE2L2, CCNE1, MYC, SMO, ERBB2, DDR2, CCND1, CDK6, CCND2, AKT1, GNA11, FBXW7 , (...)

View the complete list with 53 more genes
Specificity
5 %
Genes
28 %
Comprehensive Panel for Individualized Cancer Threatment.

By GeneKor MSA in Greece.

ROS1, ERBB4, SMO, ERBB2, DDR2, KDR, SRC, AKT1, GNA11, FBXW7, IDH1, PDGFRA, ABL1, JAK2, EGFR, NPM1, FLT3, GNAQ, CSF1R, PIK3CA , (...)

View the complete list with 32 more genes
Specificity
4 %
Genes
19 %
Circulo Breast.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Circulo Ovarian.

By Circulogene Theranostics in United States.

PIK3CA
Specificity
100 %
Genes
10 %
Solid Tumor Targeted Mutation and Fusion Panel.

By Providence Regional Laboratories Providence Health and Services in United States.

ETV1, JAK1, ERG, ESR1, FGFR4, NTRK3, ROS1, ERBB4, AXL, MYC, SMO, ERBB2, DDR2, CCND1, CDK6, NTRK2, AKT1, AKT3, GNA11, IDH1 , (...)

View the complete list with 30 more genes
Specificity
4 %
Genes
19 %
CEN4GEN Breast cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

WEE1, ACVR1B, PTGFR, ZBED4, ZNF226, TRAF5, PPM1L, MAP2K4, PCGF2, PBRM1, FBXO32, EXOC2, NCOR1, MUC16, ESR1, KMT2C, ITCH, MYC, CBFB, ERBB2 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
10 %
CEN4GEN Colorectal cancer: Extended Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MIER3, TCERG1, ATP6V0D2, ACVR1B, PTPN12, GALNT17, MAP2K4, MAP7, FZD3, MYO1B, CDC27, TCF7L2, BAX, DCC, ERBB2, MSH3, GPC6, PIK3R1, AKT1, FBXW7 , (...)

View the complete list with 18 more genes
Specificity
16 %
Genes
55 %
CEN4GEN Ovarian cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

KREMEN1, USP16, MAS1L, CSMD3, FAT3, GABRA6, CCNE1, PPP2R1A, ERBB2, CDK12, PIK3R1, AKT1, CBLC, PDGFRA, EGFR, PIK3CA, KIT, ARID1A, CTNNB1, NF1 , (...)

View the complete list with 12 more genes
Specificity
13 %
Genes
37 %
CEN4GEN Comprehensive Solid tumors (somatic genetic testing): Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

ESR1, SMO, ERBB2, AKT1, IDH1, PDGFRA, EGFR, PIK3CA, KIT, MTOR, CTNNB1, MET, CDKN2A, STK11, PTCH1, ATM, MAP2K2, FGFR2, NRAS, KRAS , (...)

View the complete list with 12 more genes
Specificity
7 %
Genes
19 %
KRAS Sequence Analysis.

By Baylor Miraca Genetics Laboratories in United States.

KRAS
Specificity
100 %
Genes
10 %
PreSeek Non-invasive Prenatal Gene Sequencing Screen.

By Baylor Miraca Genetics Laboratories in United States.

NSD1, NIPBL, TSC1, SMC1A, SMC3, SYNGAP1, CBL, RAD21, TSC2, MAP2K2, RIT1, HDAC8, SOS2, FGFR2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
10 %
Non-immune Hydrops Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

PTH1R, SEC23B, CDAN1, CCBE1, CANT1, CHRNG, NEU1, UROS, PKLR, FOXP3, SOX18, RASA1, MVK, RPS24, RPS17, RPL5, RPL11, CLCNKA, RPS10, RPS26 , (...)

View the complete list with 67 more genes
Specificity
2 %
Genes
10 %
Comprehensive Cardiac Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
10 %
Juvenile Myelomonocytic Leukemia.

By UCSF Molecular Diagnostics Laboratory University of California, San Francisco in United States.

SH2B3, JAK3, ASXL1, SETBP1, NF1, CBL, PTPN11, NRAS, KRAS
Specificity
12 %
Genes
10 %
Cardiomyopathy Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

TMPO, TXNRD2, OBSCN, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2 , (...)

View the complete list with 92 more genes
Specificity
2 %
Genes
19 %
KRAS related Noonan syndrome.

By Genetics Laboratory University of Oklahoma Health Sciences Center in United States.

KRAS
Specificity
100 %
Genes
10 %
Noonan Spectrum Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

SPRED1, NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Autoimmune Lymphoproliferative Syndrome Panel by next-generation sequencing (NGS).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

FADD, ITK, CASP10, FASLG, FAS, MAGT1, NRAS, KRAS, CASP8
Specificity
12 %
Genes
10 %
Autoimmune Lymphoproliferative Syndrome Deletion/Duplication Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

FADD, ITK, CASP10, FASLG, FAS, MAGT1, NRAS, KRAS, CASP8
Specificity
12 %
Genes
10 %
Noonan Syndrome Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Noonan Spectrum Disorders Panel, Sequencing, 15 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

SPRED1, RAB40AL, KAT6B, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
7 %
Genes
10 %
Noonan Spectrum Disorders Panel.

By GeneDx in United States.

CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
Comprehensive Cardiomyopathy Panel.

By GeneDx in United States.

MT-TL2, MT-TM, MT-TD, MT-TQ, MT-TH, MT-TI, MT-TG, TMPO, MT-ND5, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1 , (...)

View the complete list with 56 more genes
Specificity
2 %
Genes
10 %
Autism/Intellectual Disability/Multiple Anomalies.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

ERCC8, RPGRIP1L, AVPR1A, BDNF, SLC6A4, ERCC6, SPRED1, RPS6KA3, NLGN3, NLGN4X, HOXA1, AP1S2, CACNA1C, EHMT1, FOXP1, FOXP2, MED12, MID1, SHANK2, SHANK3 , (...)

View the complete list with 69 more genes
Specificity
2 %
Genes
10 %
Lynch Syndrome Paired Testing.

By Ambry Genetics in United States.

NRAS, KRAS, BRAF, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
75 %
Genes
55 %
TumorNext-Lynch+CancerNext.

By Ambry Genetics in United States.

HOXB13, DICER1, POLE, GREM1, POLD1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2 , (...)

View the complete list with 17 more genes
Specificity
17 %
Genes
55 %
TumorNext-Lynch+OvaNext.

By Ambry Genetics in United States.

DICER1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, NRAS, KRAS, TP53, PTEN, MUTYH , (...)

View the complete list with 7 more genes
Specificity
23 %
Genes
55 %
KRAS gene sequence.

By Ambry Genetics in United States.

KRAS
Specificity
100 %
Genes
10 %
Lymphedema NGS Multi-Gene Panel (36 Genes).

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

CDK19, ITGA9, PEPD, TUBGCP6, GJA1, FLT4, PTPN14, KIF11, VEGFC, ABCC9, NAGA, SPRED1, CCBE1, SOX18, FAT4, FOXC2, HGF, RELN, GATA2, MET , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
10 %
PTPN11, SOS1, RAF1, KRAS, BRAF, NRAS, HRAS, SPRED1, SHOC2, CBL, MAP2K1, MAP2K2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, RAF1
Specificity
10 %
Genes
10 %
Noonan Syndrome and Cardiofaciocutaneous Syndrome - KRAS Sequence Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

KRAS
Specificity
100 %
Genes
10 %
KRAS-Related Noonan Syndrome.

By ChildLab Molecular Genetics Laboratory Nationwide Children's Hospital in United States.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome (sequence analysis of KRAS gene).

By CGC Genetics in Portugal.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome and rasopathies (NGS panel for 13 genes).

By CGC Genetics in Portugal.

SPRED1, NF1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Non-NF1 RASopathy Next Generation Sequencing and Deletion/Duplication.

By Medical Genomics Laboratory Department of Genetics UAB in United States.

RASA2, SPRED1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
7 %
Genes
10 %
RASopathy Next Generation Sequencing and Deletion/Duplication.

By Medical Genomics Laboratory Department of Genetics UAB in United States.

SPRED1, NF1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
7 %
Genes
10 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ZBTB17, SREBF2, TRIM63, ZHX3, KLF10, TBX3, CALR3, MIB1, CAVIN4, CREB3L3, APOA4, GJA5, NPPA, GPIHBP1, APOC2, LMF1, LPL, APOA5, LDLRAP1, CETP , (...)

View the complete list with 144 more genes
Specificity
2 %
Genes
19 %
KRAS-Related Disorders via the KRAS Gene.

By PreventionGenetics PreventionGenetics in United States.

KRAS
Specificity
100 %
Genes
10 %
Fetal Concerns Sequencing Panel Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GLE1, CHRNG, KAT6B, PEX12, PEX10, PEX26, PEX6, KCNQ1, SCN5A, KCNH2, CHRND, CHRNA1, MUSK, KLHL40, RAPSN, SUMF1, SLC17A5, PEX1, DOK7, CBL , (...)

View the complete list with 20 more genes
Specificity
3 %
Genes
10 %
Autism Spectrum Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MBD6, WDFY3, DGAT2L6, CDC42BPB, SYN2, STXBP5, KAT2B, TNRC6B, TCF20, KMT5B, MYO9B, CSMD1, NAA15, DSCAM, DISC1, EFR3A, CTTNBP2, CNTN6, CTNND2, ASH1L , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
10 %
Noonan spectrum disorder NGS panel.

By Connective Tissue Gene Tests in United States.

PPP1CB, A2ML1, RRAS, RASA2, NSUN2, CABIN1, SPRED1, LZTR1, ACTG1, ACTB, NF1, NF2, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
10 %
Noonan syndrome core Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

LZTR1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Noonan syndrome core Comprehensive panel.

By Connective Tissue Gene Tests in United States.

LZTR1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Lynch Syndrome.

By MGZ Medical Genetics Center in Germany.

KRAS, BRAF, MLH1, MSH6, PMS2, MSH2
Specificity
84 %
Genes
46 %
Heart Diseases - panels.

By MGZ Medical Genetics Center in Germany.

TLL1, NKX2-6, NR2F2, MED13L, TAB2, SMAD6, TBX20, GATA5, ADAMTSL4, ZFPM2, NOTCH2, CFC1, GATA6, CRELD1, CITED2, GATA4, GDF1, GJA1, TBX5, VCL , (...)

View the complete list with 137 more genes
Specificity
2 %
Genes
19 %
Noonan Syndrome.

By MGZ Medical Genetics Center in Germany.

RRAS, RASA2, CBL, SOS1, SHOC2, PTPN11, NRAS, KRAS, RAF1
Specificity
12 %
Genes
10 %
KRAS Sequencing.

By FirmaLab in United States.

KRAS
Specificity
100 %
Genes
10 %
Congenital heart defects panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

GJC1, TBX20, CFC1, ACVR2B, CRELD1, LEFTY2, GATA4, GDF1, ZIC3, GJA1, TBX5, MYH6, NKX2-5, ACTC1, MYH11, FOXH1, NODAL, MYBPC3, LDB3, MYH7 , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
10 %
ALPS/autoimmunity panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

ITCH, IL2RA, FADD, LRBA, CASP10, FASLG, FAS, FOXP3, NRAS, KRAS, AIRE, CASP8
Specificity
9 %
Genes
10 %
Noonan syndrome type 3.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Gastric cancer, somatic.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Lung cancer, somatic.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Pancreatic carcinoma, somatic.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
10 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
10 %
Single gene testing KRAS.

By CeGaT GmbH in Germany.

KRAS
Specificity
100 %
Genes
10 %
Noonan Syndrome.

By Laboratory of Human Genetics GENOMED Health Care Center in Poland.

SOS1, PTPN11, KRAS, RAF1
Specificity
25 %
Genes
10 %
Breast and Ovarian Cancer.

By Asper Biogene Asper Biogene LLC in Estonia.

CHD1, RAD51, XRCC2, FANCD2, FANCE, FANCF, FANCG, FANCA, RAD51D, BARD1, RAD51C, BRIP1, CHEK2, STK11, PALB2, NBN, MRE11, ATM, KRAS, FANCC , (...)

View the complete list with 9 more genes
Specificity
14 %
Genes
37 %
Inherited Cardiovascular Diseases and Sudden Death Panel.

By Health in Code in Spain.

FHOD3, FOXD4, SMAD1, TRIM63, KLF10, LRP6, CALR3, MIB1, TBX20, CAVIN4, APOC3, ADAMTSL4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA , (...)

View the complete list with 193 more genes
Specificity
1 %
Genes
19 %
Cardiomyopathies Panel.

By Health in Code in Spain.

FHOD3, FOXD4, TRIM63, KLF10, CALR3, MIB1, TBX20, CAVIN4, CTNNA3, OBSL1, AGPAT2, GJA5, GATA6, CRELD1, GATA4, TMPO, TXNRD2, FHL2, CTF1, GJA1 , (...)

View the complete list with 129 more genes
Specificity
1 %
Genes
10 %
Hypertrophic Cardiomyopathy Extended Panel.

By Health in Code in Spain.

FHOD3, TRIM63, KLF10, CALR3, CAVIN4, OBSL1, AGPAT2, FHL2, CTF1, VCL, MYL3, MYL2, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
10 %
Cardiovascular Diseases_General Panel.

By Health in Code in Spain.

CH25H, BMP10, TRIB1, TOPBP1, ISL1, GREM2, HAND2, SLC25A40, NNT, PPARA, MYOM1, LPA, SLC22A8, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, SMAD1 , (...)

View the complete list with 360 more genes
Specificity
1 %
Genes
19 %
Arrhythmia General Panel.

By Health in Code in Spain.

GREM2, NNT, MYOM1, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, NKX2-6, MRPL44, KCND2, COA6, TRIM63, KLF10, PKP4, TNNI3K, CALM3, CALR3, MIB1 , (...)

View the complete list with 198 more genes
Specificity
1 %
Genes
10 %
Congenital heart diseases Panel.

By Health in Code in Spain.

ISL1, HAND2, IRX4, MCTP2, NKX2-6, MED13L, TNNI3K, TAB2, SMAD6, TFAP2B, MIB1, TBX20, GATA5, ZFPM2, NOTCH2, GJA5, TDGF1, CFC1, PDGFRA, GATA6 , (...)

View the complete list with 56 more genes
Specificity
2 %
Genes
10 %
RASopathies Panel.

By Health in Code in Spain.

A2ML1, RRAS, RASA2, SPRED1, LZTR1, NF1, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
6 %
Genes
10 %
NGS HemeOnc Panel.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States.

CSF3R, ETV6, IDH1, SF3B1, SRSF2, TET2, U2AF1, ABL1, JAK2, NPM1, FLT3, SH2B3, ASXL1, KIT, EZH2, DNMT3A, SETBP1, PHF6, MPL, CEBPA , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
CRANEO-FACIAL-CUTANEOUS SYNDROME.

By Hereditary Cancer Group - Genetic Diagnostic Unit Germans Trias I Pujol Research Institute in Spain.

MAP2K2, SOS1, MAP2K1, KRAS, BRAF
Specificity
20 %
Genes
10 %
qChip.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

SEM1, IGF2, CBFB, TRAPPC10, FBXW11, TBX3, HDAC4, TRPS1, STS, HOXD13, LMNB1, MID2, IRF6, MNX1, SIM1, DISP1, MYCN, GATA4, ZIC3, VEGFA , (...)

View the complete list with 106 more genes
Specificity
2 %
Genes
19 %
Cardiofaciocutaneous syndrome.

By MedGene in Slovakia.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome 3.

By MedGene in Slovakia.

KRAS
Specificity
100 %
Genes
10 %
Invitae Congenital Heart Defects and Heterotaxy Panel.

By Invitae in United States.

MEIS2, NKX2-6, NR2F2, MED13L, ANKS6, ZNF423, NOTCH2, CFAP53, ACVR2B, LEFTY2, GATA4, GDF1, NEK8, ZIC3, GJA1, TBX5, NKX2-5, ACTC1, DNAI1, DNAH5 , (...)

View the complete list with 62 more genes
Specificity
2 %
Genes
10 %
Invitae Congenital Heart Disease Panel.

By Invitae in United States.

HAND1, MEIS2, NKX2-6, NR2F2, MED13L, SMAD6, ZFPM2, GATA6, ACVR2B, CRELD1, LEFTY2, GATA4, GDF1, ZIC3, GJA1, TBX5, MYH6, NKX2-5, ACTC1, NOTCH1 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
10 %
Invitae Noonan Syndrome Panel.

By Invitae in United States.

A2ML1, RRAS, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
COLON, BREAST AND OVARIAN CANCER.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MLH3, AXIN2, XRCC2, NF1, RAD51D, PMS1, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, KRAS , (...)

View the complete list with 11 more genes
Specificity
26 %
Genes
73 %
KRAS Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Noonan Syndrome and Related Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
Proportionate Short Stature/Small for Gestational Age: Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SHOX2, IGF1R, IGF1, TBCE, WRN, CUL7, ROR2, SRCAP, SMARCAL1, STAT5B, INSR, TRIM37, EP300, THRB, LHX3, ERCC6, KDM6A, GLI2, SOX3, RPS6KA3 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
10 %
Cardiomyopathy: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 45 more genes
Specificity
2 %
Genes
10 %
Comprehensive Cardiovascular: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 86 more genes
Specificity
2 %
Genes
19 %
Noonan Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

EFHC2, CELSR1, GPHN, SLC6A5, GLRA1, GLRB, SCN10A, BUB1B, MAPK10, COL18A1, ACY1, MED17, SNAP29, LIG4, NHEJ1, SLC46A1, ARL13B, RPGRIP1L, PGK1, SCN4B , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
10 %
Intellectual Disability NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

AQP7, TPH2, AFP, XIST, SNIP1, ZBTB24, GLUL, DIP2B, KCNK9, UPB1, CEP57, FTO, ZBTB16, TMCO1, IRX5, AGT, IGF1R, MRAP, HDAC4, IGF1 , (...)

View the complete list with 372 more genes
Specificity
1 %
Genes
10 %
Thyroid Cancer NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SDHD, NRAS, KRAS, HRAS, BRAF, SDHB, RET, TP53, PTEN, MUTYH
Specificity
10 %
Genes
10 %
KRAS Full Gene Analysis.

By Fulgent Genetics Fulgent Genetics in United States.

KRAS
Specificity
100 %
Genes
10 %
Cardio-Facio-Cutaneous Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MAP2K2, SOS1, MAP2K1, KRAS, BRAF
Specificity
20 %
Genes
10 %
Comprehensive Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RANGAP1, EFHC2, CELSR1, NIPA2, UBR5, VDAC1, BRD2, RBFOX3, KPNA7, CNTN2, ARHGEF15, PIK3AP1, FASN, RYR3, GABBR2, HCN2, TNK2, SRGAP2, GPHN, SLC12A5 , (...)

View the complete list with 427 more genes
Specificity
1 %
Genes
10 %
Primary Immunodeficiency Panel.

By Blueprint Genetics in Finland.

BCL11B, OTULIN, IRF2BP2, RASGRP1, CARMIL2, ZNF341, TFRC, POLE2, HYOU1, JAK1, ARPC1B, BACH2, LAT, MRTFA, MSN, GINS1, CD59, ADAM17, BCL10, IRF8 , (...)

View the complete list with 255 more genes
Specificity
1 %
Genes
19 %
Hereditary Leukemia Panel.

By Blueprint Genetics in Finland.

DDX41, SAMD9L, ETV6, IKZF1, SRP72, FANCA, TERT, TERC, DKC1, NF1, CEBPA, SBDS, PAX5, GATA2, CDKN2A, NBN, ATM, CBL, MAP2K2, RIT1 , (...)

View the complete list with 19 more genes
Specificity
16 %
Genes
55 %
Comprehensive Hereditary Cancer Panel.

By Blueprint Genetics in Finland.

REST, PPM1D, EXO1, CD70, CEP57, ERCC1, MLH3, DDB2, DIS3L2, NTHL1, HOXB13, RHBDF2, CYLD, BUB1B, XPA, ERCC5, DICER1, WRN, DDX41, SAMD9L , (...)

View the complete list with 126 more genes
Specificity
6 %
Genes
73 %
Comprehensive Hematology Panel.

By Blueprint Genetics in Finland.

ARPC1B, MRTFA, GINS1, DCLRE1B, ERCC6L2, MTHFD1, AP3D1, SMARCD2, WDR1, LMAN1, MCFD2, RPS29, MECOM, TMPRSS6, F13B, SERPINC1, DHFR, F13A1, TF, F12 , (...)

View the complete list with 219 more genes
Specificity
3 %
Genes
55 %
Bone Marrow Failure Syndrome Panel.

By Blueprint Genetics in Finland.

ERCC6L2, SMARCD2, RPS29, DDX41, SAMD9L, SAMD9, DNAJC21, PGM3, ACD, JAGN1, WIPF1, CXCR4, RAC2, LAMTOR2, GFI1, RBM8A, VPS45, G6PC3, RPL15, ITK , (...)

View the complete list with 102 more genes
Specificity
5 %
Genes
55 %
Comprehensive Cardiology Panel.

By Blueprint Genetics in Finland.

PLEKHM2, PPA2, LRRC10, FBXO32, MYBPHL, CDH2, HAND1, FOXD4, TECRL, RMND1, GTPBP3, MYL4, TNNI3K, TAB2, CALM3, CALR3, ALPK3, TBX20, GATA5, RBCK1 , (...)

View the complete list with 165 more genes
Specificity
1 %
Genes
10 %
Noonan Syndrome Panel.

By Insight Medical Genetics in United States.

CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
KRAS Mutation Analysis.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

KRAS
Specificity
100 %
Genes
10 %
Focus::Myeloid™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

CBLC, BCORL1, CBLB, CSF3R, CUX1, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, NPM1 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
10 %
Focus::MDS™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

ETV6, IDH1, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, JAK2, FLT3, ASXL1, KMT2A, KDM6A, EZH2, DNMT3A, SETBP1, CEBPA, CBL, PTPN11, NRAS , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
10 %
Focus::CLL™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

XPO1, TRAF2, PIM1, HIST1H1B, HIST1H1E, IKZF3, IRF4, BIRC3, PLCG2, CARD11, POT1, MYD88, SF3B1, NOTCH1, ZMYM3, MED12, BTK, CDKN2A, ATM, NRAS , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
10 %
Hypertrophic Cardiomyopathy Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

MYL3, MYL2, CSRP3, ACTN2, MYOZ2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, LAMP2, MYBPC3, MYH7, MAP2K2, RIT1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
Severe Congenital Neutropenia Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

CXCR2, JAGN1, CXCR4, LAMTOR2, GFI1, VPS45, G6PC3, ELANE, CSF3R, RAB27A, USB1, LYST, VPS13B, WAS, SBDS, GATA2, NRAS, KRAS, TCIRG1, TAZ , (...)

View the complete list with 4 more genes
Specificity
5 %
Genes
10 %
Thoracic Tumors Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

KMT2C, ROS1, KEAP1, ERBB2, DDR2, KDR, FLT1, AKT1, AKT3, AKT2, CDKN1B, BAP1, FANCA, FLT4, SMARCA4, ERBB3, MED12, KMT2D, FGFR1, NF1 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
10 %
Noonan Syndrome Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CBL, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
12 %
Genes
10 %
Circulo Breast.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Colorectal.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Ovarian.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Melanoma.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Thyroid.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Hematological.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Pancreatic.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Circulo Gastric.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
LEUKEMIA, ACUTE MYELOGENOUS.

By Laboratorio de Genetica Clinica SL in Spain.

NPM1, KRAS
Specificity
50 %
Genes
10 %
PANCREATIC CARCINOMA.

By Laboratorio de Genetica Clinica SL in Spain.

KRAS
Specificity
100 %
Genes
10 %
Cardiofaciocutaneous Syndrome Type 2, Sequencing KRAS Gene.

By Reference Laboratory Genetics in Spain.

KRAS
Specificity
100 %
Genes
10 %
Cardio-facio-cutaneous syndrome.

By Labor Dr. Wisplinghoff in Germany.

MAP2K2, KRAS, BRAF
Specificity
34 %
Genes
10 %
Phosphorus Pan Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 49 more genes
Specificity
2 %
Genes
10 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 67 more genes
Specificity
2 %
Genes
10 %
Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, A2ML1, RRAS, SPRED1, LAMP2, RASA1, CACNA1C, TCAP, MYBPC3 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
10 %
GeneStrat Genomic Test.

By Biodesix, Inc. Biodesix, Inc. in United States.

ROS1, EGFR, ALK, KRAS, BRAF, RET
Specificity
17 %
Genes
10 %
KRAS Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories in United States.

KRAS
Specificity
100 %
Genes
10 %
KRAS Sequence Analysis (Prenatal Diagnosis).

By Baylor Miraca Genetics Laboratories in United States.

KRAS
Specificity
100 %
Genes
10 %
KRAS/RAF1/SOS1 DNA Sequencing Evaluation.

By Athena Diagnostics Inc in United States.

SOS1, KRAS, RAF1
Specificity
34 %
Genes
10 %
KRAS DNA Sequencing Test.

By Athena Diagnostics Inc in United States.

KRAS
Specificity
100 %
Genes
10 %
NGS RASopathy Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

A2ML1, RRAS, RASA2, NSUN2, CABIN1, SPRED1, KAT6B, LZTR1, NF1, NF2, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
Cardiofaciocutaneous Syndrome.

By Center for Human Genetics, Inc in United States.

MAP2K2, MAP2K1, KRAS, BRAF
Specificity
25 %
Genes
10 %
Cardio-facio-cutaneous syndrome.

By Center for Human Genetics, Inc in United States.

MAP2K2, MAP2K1, KRAS, BRAF
Specificity
25 %
Genes
10 %
Noonan syndrome 3 (KRAS).

By Center for Human Genetics, Inc in United States.

KRAS
Specificity
100 %
Genes
10 %
Costello Syndrome.

By Center for Human Genetics, Inc in United States.

KRAS, HRAS, BRAF
Specificity
34 %
Genes
10 %
Noonan Syndrome 11-Gene Sequencing Panel.

By Center for Human Genetics, Inc in United States.

LZTR1, CBL, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, KRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
Rasopathy NextGen Panel.

By Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado in United States.

PPP1CB, A2ML1, RRAS, RASA2, SPRED1, LZTR1, ACTG1, ACTB, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Noonan Syndrome Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
KRAS Mutation Analysis.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories in United States.

KRAS
Specificity
100 %
Genes
10 %
MyeloidDx by NGS.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories in United States.

BCORL1, CBLB, CSF3R, CUX1, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, NPM1, FLT3 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
10 %
MyeloidDx by NGS.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories in United States.

TET2-AS1, CBLC, BCORL1, CBLB, CSF3R, CUX1, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, U2AF1, ZRSR2, ABL1, JAK2, NPM1 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
10 %
KRAS Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

KRAS
Specificity
100 %
Genes
10 %
KRAS Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

KRAS
Specificity
100 %
Genes
10 %
Prenatal Noonan Spectrum Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

MAP2K2, RIT1, SOS1, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
Noonan Syndrome Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

NF1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
KRAS Molecular Genetic Testing.

By Michigan State University Clinical Genetics Laboratory Michigan State University in United States.

KRAS
Specificity
100 %
Genes
10 %
Expanded RASopathy Panel (14 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

SPRED1, NF1, CBL, MAP2K2, RIT1, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
KRAS-Related Noonan Syndrome.

By Molecular Diagnostics Lab Nemours Alfred I. duPont Hospital for Children in United States.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome/RASopathy Disorders Panel.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
Noonan Syndrome Panel.

By Ambry Genetics in United States.

SOS1, PTPN11, KRAS, RAF1
Specificity
25 %
Genes
10 %
TumorNext-Lynch+ColoNext.

By Ambry Genetics in United States.

POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, NRAS, KRAS, BRAF, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
30 %
Genes
55 %
TumorNext-Lynch.

By Ambry Genetics in United States.

NRAS, KRAS, BRAF, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
75 %
Genes
55 %
KRAS. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KRAS
Specificity
100 %
Genes
10 %
PTPN11, RAF1, SOS1, KRAS, BRAF. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SOS1, PTPN11, KRAS, RAF1
Specificity
25 %
Genes
10 %
KRAS-Related Noonan Syndrome.

By Unity of Clinical Genetics and Functional Genomics University of Zaragoza. Faculty of Medicine. in Spain.

KRAS
Specificity
100 %
Genes
10 %
Noonan Spectrum Panel - PTPN11, RAF1, SOS1, KRAS, BRAF, HRAS, NRAS, CBL, SHOC2, MAP2K1, MAP2K2, and SPRED1 Next Generation Sequence Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
Noonan Syndrome Seq Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
KRAS gene (sequence analysis).

By CGC Genetics in Portugal.

KRAS
Specificity
100 %
Genes
10 %
Detection of frequent mutations on KRAS gene.

By CGC Genetics in Portugal.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome (NGS panel for 5 genes).

By CGC Genetics in Portugal.

SOS1, PTPN11, NRAS, KRAS, RAF1
Specificity
20 %
Genes
10 %
Peripheral Nerve Sheath Tumor NGS panel.

By Medical Genomics Laboratory Department of Genetics UAB in United States.

SMARCB1, LZTR1, NF1, NF2, PTPN11, KRAS
Specificity
17 %
Genes
10 %
Noonan Spectrum Disorders/Rasopathies Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MAP3K8, SPRY1, A2ML1, RRAS, RASA2, KAT6B, LZTR1, NF1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Hypertrophic Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, MYLK2, ACTC1, RYR2 , (...)

View the complete list with 18 more genes
Specificity
3 %
Genes
10 %
Pan Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CALR3, MIB1, CAVIN4, TMPO, FHL2, DPP6, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN , (...)

View the complete list with 62 more genes
Specificity
3 %
Genes
19 %
Autoimmune Lymphoproliferative Syndrome/ALPS Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

PRKCD, CTLA4, FADD, LRBA, PIK3CD, ITK, CASP10, FASLG, XIAP, FAS, SH2D1A, MAGT1, NRAS, KRAS, STAT3, CASP8
Specificity
7 %
Genes
10 %
Noonan spectrum disorder Comprehensive panel.

By Connective Tissue Gene Tests in United States.

PPP1CB, A2ML1, RRAS, RASA2, NSUN2, CABIN1, SPRED1, LZTR1, ACTG1, ACTB, NF1, NF2, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
10 %
Noonan spectrum disorder Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

PPP1CB, A2ML1, RRAS, RASA2, NSUN2, CABIN1, SPRED1, LZTR1, ACTG1, ACTB, NF1, NF2, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
10 %
Noonan syndrome core NGS panel.

By Connective Tissue Gene Tests in United States.

LZTR1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Hypertrophic cardiomyopathy - different panels.

By Institute of Human Genetics Cologne University in Germany.

AGPAT2, MYL3, MYL2, CSRP3, TNNT2, TPM1, PLN, PRKAG2, TNNI3, ACTC1, LAMP2, LZTR1, ACTA1, MYBPC3, FHL1, BSCL2, MYH7, DES, TTN, NF1 , (...)

View the complete list with 45 more genes
Specificity
2 %
Genes
10 %
Noonan syndrome - different panels.

By Institute of Human Genetics Cologne University in Germany.

A2ML1, RRAS, RASA2, LZTR1, RIT1, SOS2, SOS1, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
RASopathies.

By MGZ Medical Genetics Center in Germany.

RRAS, RASA2, SPRED1, NF1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
7 %
Genes
10 %
Cardiofaciocutaneous Syndrome Panel.

By FirmaLab in United States.

MAP2K2, KRAS, BRAF
Specificity
34 %
Genes
10 %
Noonan Syndrome Sequential Panel.

By FirmaLab in United States.

SOS1, PTPN11, KRAS, RAF1
Specificity
25 %
Genes
10 %
Myeloid Tumor Panel.

By Centogene AG - the Rare Disease Company in Germany.

CBLC, BCORL1, CBLB, CSF3R, CUX1, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, NPM1 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
10 %
Breast cancer, somatic.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Bladder cancer, somatic.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Cardiofaciocutaneous syndrome.

By Centogene AG - the Rare Disease Company in Germany.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

SOS1, PTPN11, KRAS, BRAF, RAF1
Specificity
20 %
Genes
10 %
Noonan Syndrome.

By Laboratory of Human Genetics GENOMED Health Care Center in Poland.

SOS1, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
15 %
Genes
10 %
Bladder cancer, somatic (KRAS).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KRAS
Specificity
100 %
Genes
10 %
Cardiofaciocutaneous syndrome 2 (KRAS).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KRAS
Specificity
100 %
Genes
10 %
Noonan Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

SPRED1, KAT6B, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
8 %
Genes
10 %
Rasopathies SANGER Panel.

By Health in Code in Spain.

MAP2K2, MAP2K1, KRAS, BRAF
Specificity
25 %
Genes
10 %
KRAS gene sequencing.

By Health in Code in Spain.

KRAS
Specificity
100 %
Genes
10 %
Hypertrophic cardiomyopathy with suspected Noonan Syndrome.

By Health in Code in Spain.

PTPN11, KRAS
Specificity
50 %
Genes
10 %
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease.

By Health in Code in Spain.

FHOD3, TRIM63, KLF10, CALR3, CAVIN4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA, GATA6, GATA4, FHL2, CTF1, GJA1, TBX5, VCL , (...)

View the complete list with 121 more genes
Specificity
1 %
Genes
10 %
Rasopathies NGS Panel.

By Health in Code in Spain.

SPRED1, CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
9 %
Genes
10 %
Congenital Heart Diseases Panel.

By Health in Code in Spain.

TBX20, GJA5, GATA6, CRELD1, GATA4, GJA1, TBX5, DTNA, NEXN, MYH6, TNNI3, ANKRD1, NKX2-5, ACTC1, KCNJ8, MYH11, ACTA2, SMAD3, NOTCH1, TBX1 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
10 %
Hypertrophic cardiomyopathy extended panel.

By Health in Code in Spain.

MYOM1, FHOD3, MRPL44, COA6, TRIM63, KLF10, CALR3, CAVIN4, COA5, OBSL1, AGPAT2, OBSCN, FHL2, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2 , (...)

View the complete list with 84 more genes
Specificity
1 %
Genes
10 %
Cardiomyopathies General Panel.

By Health in Code in Spain.

NNT, MYOM1, PPP1R13L, PERP, FHOD3, FOXD4, MRPL44, COA6, TRIM63, KLF10, PKP4, TNNI3K, CALR3, MIB1, TBX20, CAVIN4, CHRM2, GATA5, CTNNA3, COA5 , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
10 %
Primary lymphedema and Hydrops fetalis.

By Center for Human Genetics Cliniques Universitaires Saint Luc in Belgium.

EPHB4, ITGA9, GJA1, FLT4, PTPN14, KIF11, VEGFC, CCBE1, SOX18, RASA1, FAT4, PIEZO1, FOXC2, HGF, GATA2, SOS1, PTPN11, NRAS, KRAS, IKBKG , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
Cardiofaciocutaneous syndrome.

By Praxis fuer Humangenetik Wien in Austria.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome 3.

By Praxis fuer Humangenetik Wien in Austria.

KRAS
Specificity
100 %
Genes
10 %
RASOPATHY-RELATED SYNDROME.

By Hereditary Cancer Group - Genetic Diagnostic Unit Germans Trias I Pujol Research Institute in Spain.

A2ML1, RRAS, RASA2, SPRED1, LZTR1, NF1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
6 %
Genes
10 %
NOONAN SYNDROME.

By Hereditary Cancer Group - Genetic Diagnostic Unit Germans Trias I Pujol Research Institute in Spain.

A2ML1, RRAS, RASA2, LZTR1, NF1, CBL, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
7 %
Genes
10 %
Invitae Cardio-Facio-Cutaneous Syndrome Panel.

By Invitae in United States.

MAP2K2, SOS1, SHOC2, MAP2K1, KRAS, BRAF
Specificity
17 %
Genes
10 %
Invitae RASopathies Comprehensive Panel.

By Invitae in United States.

A2ML1, RRAS, SPRED1, RASA1, NF1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
6 %
Genes
10 %
KRAS: KRAS gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KRAS
Specificity
100 %
Genes
10 %
Noonan syndrome 3: KRAS gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KRAS
Specificity
100 %
Genes
10 %
KRAS Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

KRAS
Specificity
100 %
Genes
10 %
Comprehensive Cardiovascular: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CTNNA3, GJA5, NPPA, TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN , (...)

View the complete list with 97 more genes
Specificity
2 %
Genes
19 %
Cardiomyopathy: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 42 more genes
Specificity
2 %
Genes
10 %
Noonan Syndrome and Related Conditions Profile.

By Integrated Genetics Westborough Integrated Genetics in United States.

MAP2K2, SOS1, SHOC2, PTPN11, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
12 %
Genes
10 %
Short Stature NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

EP300, FGD1, NIPBL, SMC1A, SOS1, PTPN11, KRAS, DHCR7, CREBBP, RAF1
Specificity
10 %
Genes
10 %
Hypertrophic Cardiomyopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TMPO, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN , (...)

View the complete list with 43 more genes
Specificity
2 %
Genes
10 %
KRAS.

By Fulgent Genetics Fulgent Genetics in United States.

KRAS
Specificity
100 %
Genes
10 %
BREASTON-EXTENDED.

By PentaCoreLab in Hungary.

DIRAS3, ERBB2, RAD51, BARD1, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, ATM, KRAS, TP53, BRCA2, BRCA1
Specificity
7 %
Genes
10 %
Onco microarray for MDS/AML.

By Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center in United States.

SET, ELL, GAS6, AFF1, ACSL6, ARHGAP26, AFDN, MLLT10, MRTFA, NUP98, ELF4, ERG, FOXO4, MYB, RBM15, EGR1, MECOM, RPN1, MLLT1, MLLT3 , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
10 %
Cardiomyopathy Panel.

By Blueprint Genetics in Finland.

PLEKHM2, PPA2, LRRC10, FBXO32, MYBPHL, CDH2, HAND1, FOXD4, RMND1, GTPBP3, MYL4, TNNI3K, TAB2, CALR3, ALPK3, TBX20, RBCK1, CTNNA3, EPG5, XK , (...)

View the complete list with 135 more genes
Specificity
1 %
Genes
10 %
Comprehensive Short Stature Syndrome Panel.

By Blueprint Genetics in Finland.

IRS1, IGFALS, IGF1R, TBX3, IGF1, POC1A, LARP7, CCDC8, OBSL1, XRCC4, RNU4ATAC, ORC4, ORC6, CDT1, CDC6, ORC1, CDC45, CEP63, CUL7, RTTN , (...)

View the complete list with 55 more genes
Specificity
2 %
Genes
10 %
Hereditary Pediatric Cancer Panel.

By Blueprint Genetics in Finland.

REST, DIS3L2, BUB1B, DICER1, WRN, AXIN2, BAP1, SMARCB1, SMARCA4, EZH2, RRAS, RASA2, NSUN2, LZTR1, NF1, CDC73, PRKAR1A, PRF1, CEBPA, PAX5 , (...)

View the complete list with 51 more genes
Specificity
9 %
Genes
55 %
Noonan Syndrome Panel.

By Blueprint Genetics in Finland.

PPP1CB, RRAS, RASA2, NSUN2, SPRED1, LZTR1, ACTG1, ACTB, NF1, CBL, MAP2K2, RIT1, SOS2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
Anti-EGFR antibody therapy response in metastatic colorectal Carcinoma.

By HeartGenetics, Genetics and Biotechnology, SA in Portugal.

NRAS, KRAS, BRAF
Specificity
34 %
Genes
10 %
KRAS Mutation by PCR.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

KRAS
Specificity
100 %
Genes
10 %
Focus::Myeloid™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

CBLC, CBLB, CSF3R, ETV6, FBXW7, IDH1, IKZF1, MYD88, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ABL1, JAK2, NPM1, FLT3, GNAS, CALR , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
10 %
Focus::AML™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

BCORL1, CSF3R, ETV6, IDH1, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2, NPM1, FLT3, CALR, ASXL1, KIT, KMT2A, KDM6A, EZH2 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
10 %
Focus::DLBCL&FL™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

FOXO1, SGK1, STAT6, SYK, SOCS1, PIM1, PRDM1, IKZF3, IRF4, BCL10, GNAI2, GNA13, MYC, BCL6, CDKN2B, BCL2, CD79B, CD79A, B2M, PLCG2 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
10 %
Focus::Lymphoma™ NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

FOXO1, SGK1, STAT6, SYK, SOCS1, PIM1, PRDM1, IKZF3, CCND3, IRF4, BCL10, IRF8, KMT2C, GNAI2, GNA13, MYC, BCL6, CDKN2B, BCL2, CCND1 , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
10 %
V-KI-RAS2 Kirsten rat sarcoma viral oncogene Homolog V-KI-RAS-2.

By Bioarray in Spain.

KRAS
Specificity
100 %
Genes
10 %
Lung and colon cancer.

By Bioarray in Spain.

KRAS
Specificity
100 %
Genes
10 %
CardioGene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TMPO, FHL2, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2 , (...)

View the complete list with 60 more genes
Specificity
2 %
Genes
10 %
Cardiomyopathy Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TMPO, FHL2, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2 , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
10 %
Hematopoietic Disorders Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TSLP, FGFR4, TET1, BIRC3, PDGFRB, NOTCH2, IL7R, CSF3R, ETV6, FBXW7, IDH1, PDGFRA, SF3B1, SRSF2, STAG2, TET2, U2AF1, ZRSR2, ABL1, JAK2 , (...)

View the complete list with 34 more genes
Specificity
2 %
Genes
10 %
Cardiofaciocutaneous Syndrome Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

MAP2K2, MAP2K1, KRAS, BRAF
Specificity
25 %
Genes
10 %
Noonan Syndrome and related disorders (RASopathies) Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CBL, MAP2K2, SOS1, SHOC2, PTPN11, NRAS, MAP2K1, KRAS, HRAS, BRAF, RAF1
Specificity
10 %
Genes
10 %
KRAS Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KRAS
Specificity
100 %
Genes
10 %
Exome.

By DNA CONSULT GENETICA E BIOTECNOLOGIA LTDA. in Brazil.

IPW, SMNDC1, GEMIN2, HERC2, ATXN8, CYP2C9, IL1RN, CCDC88C, VKORC1, CYP2D6, CYP2C19, F8, F9, MAGEL2, SOX9, RPL10, PTCHD1, SEMA3E, SHANK2, KCND3 , (...)

View the complete list with 46 more genes
Specificity
2 %
Genes
10 %
Cardiomyopathy Exome Panel.

By Northwest Clinical Genomics Laboratory University of Washington in United States.

CAVIN4, CHRM2, TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 55 more genes
Specificity
2 %
Genes
10 %
Circulo Lung.

By Circulogene Theranostics in United States.

KRAS
Specificity
100 %
Genes
10 %
LUNG CANCER, SQUAMOUS CELL.

By Laboratorio de Genetica Clinica SL in Spain.

KRAS
Specificity
100 %
Genes
10 %
CARDIOFACIOCUTANEOUS SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

MAP2K2, MAP2K1, KRAS, BRAF
Specificity
25 %
Genes
10 %
NOONAN SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

SOS1, PTPN11, NRAS, MAP2K1, KRAS, BRAF, RAF1
Specificity
15 %
Genes
10 %
BLADDER CANCER.

By Laboratorio de Genetica Clinica SL in Spain.

KRAS
Specificity
100 %
Genes
10 %
Noonan Syndrome Type 3, Sequencing KRAS Gene.

By Reference Laboratory Genetics in Spain.

KRAS
Specificity
100 %
Genes
10 %
Familial Pancreatic Cancer , Panel Massive Sequencing (NGS) 16 Genes.

By Reference Laboratory Genetics in Spain.

MLH3, TGFBR2, SMAD4, CDKN2A, STK11, PALB2, KRAS, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, BRCA2, BRCA1
Specificity
44 %
Genes
64 %
Juvenile Myelomonocytic Leukemia , Panel Massive Sequencing (NGS) 5 Genes.

By Reference Laboratory Genetics in Spain.

NF1, CBL, PTPN11, NRAS, KRAS
Specificity
20 %
Genes
10 %
Cardiofaciocutaneous Syndrome , Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

MAP2K2, SOS1, SHOC2, MAP2K1, KRAS, BRAF
Specificity
17 %
Genes
10 %
Acute Myeloid Leukemia (Susceptibility to) , Panel Massive Sequencing (NGS) 21 Genes.

By Reference Laboratory Genetics in Spain.

SH3GL1, LPP, CBFB, PICALM, IDH1, JAK2, NPM1, FLT3, ASXL1, KIT, TERT, TERC, DNMT3A, CEBPA, GATA2, NSD1, KRAS, IDH2, WT1, TP53 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Autosomic Autoimmune Lymphoproliferative Syndrome , Panel Massive Sequencing (NGS) 10 Genes.

By Reference Laboratory Genetics in Spain.

CTLA4, FADD, ITK, CASP10, FASLG, FAS, MAGT1, NRAS, KRAS, CASP8
Specificity
10 %
Genes
10 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 75 more genes
Specificity
2 %
Genes
10 %
Phosphorus Pan Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
10 %
Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, A2ML1, RRAS, SPRED1, LAMP2, RASA1, CACNA1C, TCAP, FHL1, BAG3, LDB3, FLNC , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
10 %
Comprehensive Hereditary Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

RAD51D, PMS1, ENG, BARD1, RAD51C, CDC73, PRKAR1A, PRF1, CEBPA, SBDS, PAX5, GATA2, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, GPC3, MET , (...)

View the complete list with 41 more genes
Specificity
10 %
Genes
55 %
Hereditary nonpolyposis colon cancer (sequence analysis of PMS1 gene).

By CGC Genetics in Portugal.

PMS1
Specificity
100 %
Genes
10 %
Colorectal Cancer.

By MGZ Medical Genetics Center in Germany.

BUB1B, PMS1, SMAD4, BMPR1A, CHEK2, MET, STK11, NBN, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC
Specificity
32 %
Genes
46 %
Hnpcc Deep Intronic.

By MGZ Medical Genetics Center in Germany.

MSH3, MLH3, PMS1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
88 %
Genes
64 %
Nonpolyposis colon cancer.

By Centogene AG - the Rare Disease Company in Germany.

PMS1
Specificity
100 %
Genes
10 %
ONCOLOGY, PANEL.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

POLH, XPC, HOXB13, XPA, ERCC5, AIP, ELANE, PDGFRA, GREM1, ERCC4, CDKN1B, XRCC2, FANCD2, FANCI, FANCL, SLX4, FANCE, FANCF, FANCG, FANCA , (...)

View the complete list with 60 more genes
Specificity
7 %
Genes
46 %
Hereditary Colorectal/Gastrointestinal Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

PMS1, ENG, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC , (...)

View the complete list with 2 more genes
Specificity
28 %
Genes
55 %
PMS1. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PMS1
Specificity
100 %
Genes
10 %
Hereditary Cancer Syndromes - panels.

By MGZ Medical Genetics Center in Germany.

RNF43, CEP57, DDB2, DIS3L2, XPC, NTHL1, RHBDF2, CYLD, BUB1B, XPA, ERCC5, DICER1, WRN, AIP, EXT1, EXT2, AXIN2, POLE, EGFR, GREM1 , (...)

View the complete list with 80 more genes
Specificity
6 %
Genes
55 %
Gastric Cancer.

By MGZ Medical Genetics Center in Germany.

PMS1, BMPR1A, CHEK2, STK11, CDH1, TP53, MLH1, MSH6, PMS2, MSH2
Specificity
50 %
Genes
46 %
Pancreatic Cancer.

By MGZ Medical Genetics Center in Germany.

PMS1, CHEK2, CDKN2A, STK11, PALB2, PTEN, MLH1, MSH6, PMS2, MSH2, BRCA2
Specificity
46 %
Genes
46 %
Breast and Ovarian Cancer - extended Diagnostic Panel.

By CeGaT GmbH in Germany.

UIMC1, RINT1, MSH3, ABRAXAS1, XRCC2, FANCD2, SLX4, FANCE, FANCF, FANCG, FANCA, NF1, RAD51D, PMS1, BARD1, RAD51C, BRIP1, RAD50, CHEK2, SDHD , (...)

View the complete list with 21 more genes
Specificity
15 %
Genes
55 %
COLON CANCER.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MSH3, PMS1, ENG, SMAD4, BMPR1A, FLCN, STK11, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
40 %
Genes
55 %
Colon Cancer NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

EXO1, GALNT12, BUB1B, AXIN2, PMS1, SMAD4, BMPR1A, CHEK2, FLCN, CDKN2A, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 1 more genes
Specificity
29 %
Genes
55 %
Hereditary Cancer NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RBM15, EXO1, XRCC3, PICALM, ROBO2, MSH3, DDB2, XPC, HOXB13, CYLD, GALNT12, BUB1B, RAD51, XPA, ERCC5, DICER1, EGLN1, WRN, PRKDC, AIP , (...)

View the complete list with 92 more genes
Specificity
6 %
Genes
55 %
PMS1.

By Fulgent Genetics Fulgent Genetics in United States.

PMS1
Specificity
100 %
Genes
10 %
Comprehensive Cancer Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RBM15, EXO1, XRCC3, PICALM, ROBO2, MSH3, DDB2, DIS3L2, XPC, HOXB13, CYLD, GALNT12, BUB1B, RAD51, XPA, ERCC5, DICER1, EGLN1, WRN, PRKDC , (...)

View the complete list with 104 more genes
Specificity
5 %
Genes
55 %
Hereditary nonpolyposis colorectal cancer.

By Bioarray in Spain.

PMS1
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer (metilation analysis and deletions/duplications analysis of MLH1, MLH3, MSH2, MSH3, MSH6, PMS2 and MGMT by MS-MLPA).

By CGC Genetics in Portugal.

MSH3, MLH3, MLH1, MSH6, PMS2, MSH2
Specificity
84 %
Genes
46 %
Hereditary colorectal cancer.

By Laboratory of Genetics HUSLAB in Finland.

MLH3, POLE, POLD1, SMAD4, BMPR1A, STK11, MUTYH, MLH1, MSH6, PMS2, MSH2, APC
Specificity
42 %
Genes
46 %
Lynch Syndrome via MLH3 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MLH3
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis type 7.

By Centogene AG - the Rare Disease Company in Germany.

MLH3
Specificity
100 %
Genes
10 %
MMR genes methylation analysis.

By Centogene AG - the Rare Disease Company in Germany.

MSH3, MLH3, MGMT, MLH1, MSH6, PMS2, MSH2
Specificity
72 %
Genes
46 %
MLH3.

By Fulgent Genetics Fulgent Genetics in United States.

MLH3
Specificity
100 %
Genes
10 %
Colorectal Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MLH3, GALNT12, AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
32 %
Genes
55 %
Hereditary Non-Polyposis Colon Cancer , Sequencing MLH3 Gene.

By Reference Laboratory Genetics in Spain.

MLH3
Specificity
100 %
Genes
10 %
Nonpolyposis hereditary colorectal cancer (sequence analysis of MLH3 gene).

By CGC Genetics in Portugal.

MLH3
Specificity
100 %
Genes
10 %
Hereditary colon cancer (panel NGS of 21 genes).

By CGC Genetics in Portugal.

MSH3, MLH3, GALNT12, AXIN2, POLE, POLD1, TGFBR2, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 1 more genes
Specificity
34 %
Genes
64 %
Hereditary nonpolyposis colorectal cancer (metilation analysis and deletions/duplications analysis of MLH1, MLH3, MSH2, MSH3, MSH6, PMS2 and MGMT by MS-MLPA).

By CGC Genetics in Portugal.

MSH3, MLH3, MLH1, MSH6, PMS2, MSH2
Specificity
84 %
Genes
46 %
Hereditary colon cancer (panel NGS of 21 genes).

By CGC Genetics in Portugal.

MSH3, MLH3, GALNT12, AXIN2, POLE, POLD1, TGFBR2, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 1 more genes
Specificity
34 %
Genes
64 %
COLORECTAL CANCER, NONPOLYPOSIC (LYNCH SYNDROME).

By Laboratorio de Genetica Clinica SL in Spain.

MLH3, MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
46 %
Loeys-Dietz Syndrome (TGFßR1, TGFßR2, SMAD3, and TGFß2).

By Center for Human Genetics, Inc in United States.

TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
25 %
Genes
10 %
Loeys-Dietz syndrome - full panel.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, SMAD4
Specificity
17 %
Genes
10 %
Loeys-Dietz syndrome - familial variant analysis.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, SMAD4
Specificity
17 %
Genes
10 %
Familial Aneurysm Panel.

By Collagen Diagnostic Laboratory University of Washington in United States.

BGN, LOX, SMAD2, MAT2A, MFAP5, PRKG1, TGFB3, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, SMAD4, CBS , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
Marfan Syndrome and Loeys-Dietz Syndrome Panel.

By Collagen Diagnostic Laboratory University of Washington in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
17 %
Genes
10 %
Marfan Syndrome, Type 2 - TGFBR2 Gene.

By Center for Genetics at Saint Francis Saint Francis Hospital in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Connective Tissue Disorders Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
Familial Aneurysm and Aortopathy.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

B3GALT6, TGFB3, ZNF469, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
Marfan Syndrome and MFS Related Disorders Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Thoracic Aortic Aneurysm Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, FLNA, CBS, FBN1, COL3A1
Specificity
8 %
Genes
10 %
Loeys-Dietz Syndrome (TGFBR1 and TGFBR2) Sequencing.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Aortopathy Panel, Sequencing and Deletion/Duplication, 21 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

PRKG1, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, FLNA, SMAD4, PLOD1, COL5A2, COL5A1, CBS, PLOD3, FBN1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Marfan/TAAD Sequencing & Del/Dup Panel.

By GeneDx in United States.

MYH11, SLC2A10, ACTA2, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, MED12, FLNA, COL5A2, COL5A1, CBS, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Connective Tissue Disorders Panel.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

ADAMTS10, SMAD2, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
10 %
COL3A1 gene sequence and deletion/duplication reflex TAADNext.

By Ambry Genetics in United States.

PRKG1, TGFB3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, SMAD4, PLOD1, COL5A2, COL5A1, CBS , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
FBN1 gene sequence and deletion/duplication reflex TAADNext.

By Ambry Genetics in United States.

PRKG1, TGFB3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, SMAD4, PLOD1, COL5A2, COL5A1, CBS , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
Loeys Dietz syndrome.

By Human Genetics University Hospital Bern in Switzerland.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR1, TGFBR2, FBN1, ACTA2, FBN2, ELN, TGFBR3. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR3, ACTA2, FBN2, TGFBR2, TGFBR1, FBN1, ELN
Specificity
15 %
Genes
10 %
FBN1, TGFBR2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2, FBN1
Specificity
50 %
Genes
10 %
TGFBR1, TGFBR2. MLPA testing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
FBN1, TGFBR1, TGFBR2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
TGFBR2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Pneumothorax Seq + Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

TGFBR2, TGFBR1, FLCN, FBN1, COL3A1
Specificity
20 %
Genes
10 %
Connective Tissue Seq Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
10 %
Connective Tissue Seq + Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
10 %
Craniosynostosis (NGS panel for 30 genes).

By CGC Genetics in Portugal.

TMCO1, IRX5, IMPAD1, TCF12, ERF, MEGF8, ESCO2, BMP4, FREM1, IFT122, IL11RA, MASP1, EFNB1, ALX4, SCARF2, WDR19, IFT140, GLI3, SKI, TGFBR2 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
10 %
Marfan syndrome type 2 (sequence analysis of TGFBR1 and TGFBR2 genes).

By CGC Genetics in Portugal.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer, type 6 (HNPCC6, sequence analysis of TGFBR2 gene).

By CGC Genetics in Portugal.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome (deletion/duplication analysis on TGFBR1 and TGFBR2 genes).

By CGC Genetics in Portugal.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Marfan and Loeys-Dietz syndromes (NGS panel for 3 genes).

By CGC Genetics in Portugal.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Skeletal Disorders and Joint Problems Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TGDS, DDX59, COL27A1, SULF1, NPPC, TXNL4A, TBX4, RASGRP2, KIF22, ADAMTS17, ACAN, PAPSS2, LMBR1, NOG, FMN1, FBXW4, FBLN1, GHSR, TBX6, XYLT1 , (...)

View the complete list with 238 more genes
Specificity
1 %
Genes
10 %
Craniosynostosis Comprehensive panel.

By Connective Tissue Gene Tests in United States.

CYP26B1, SLC25A24, TCF12, ERF, ZIC1, MEGF8, CDC45, FREM1, IFT122, IL11RA, IFT43, EFNB1, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
10 %
Craniosynostosis NGS panel.

By Connective Tissue Gene Tests in United States.

CYP26B1, SLC25A24, TCF12, ERF, ZIC1, MEGF8, CDC45, FREM1, IFT122, IL11RA, IFT43, EFNB1, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
10 %
Loeys-Dietz syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Loeys-Dietz syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

BGN, LOX, SMAD2, MAT2A, MFAP5, PRKG1, TGFB3, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome core NGS panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Loeys-Dietz syndrome core Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

BGN, LOX, SMAD2, MAT2A, MFAP5, PRKG1, TGFB3, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
10 %
Marfan syndrome, type I / II NGS panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, FBN1
Specificity
50 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
17 %
Genes
10 %
Marfan syndrome, type I / II Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, FBN1
Specificity
50 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
17 %
Genes
10 %
Loeys-Dietz syndrome 2 Deletion / Duplication test.

By Connective Tissue Gene Tests in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Thoracic aortic diseases.

By Institute of Human Genetics Cologne University in Germany.

MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, CBS, FBN1, COL3A1
Specificity
10 %
Genes
10 %
Marfan syndrome, EDS and other connective tissue disorders - different panels.

By Institute of Human Genetics Cologne University in Germany.

GATA5, DSE, B3GALT6, MAT2A, MFAP5, PRKG1, TGFB3, EFEMP2, CHST14, TNXB, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
10 %
Thoracic Aortic Aneurysms and Aortic Dissections (TAAD).

By MGZ Medical Genetics Center in Germany.

PRKG1, EFEMP2, MYH11, SLC2A10, ACTA2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, CBS, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Cardiovascular disorders panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

SLC8A1, TGFB3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, COL5A2, COL5A1, CBS, FBN1, ELN, COL3A1
Specificity
6 %
Genes
10 %
Aortic Aneurysm, familial thoracic type 1.

By Centogene AG - the Rare Disease Company in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome type 1B.

By Centogene AG - the Rare Disease Company in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis type 6.

By Centogene AG - the Rare Disease Company in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan, Loeys-Dietz syndrome and related disorders panel.

By Centogene AG - the Rare Disease Company in Germany.

SMAD2, TGFB3, EFEMP2, SLC2A10, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL5A2, COL5A1, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Connective tissue disorders - Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, Aortic Aneurysm.

By CeGaT GmbH in Germany.

DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
10 %
Thoracic Aortic Aneurysms and Aortic Dissections.

By Laboratory of Human Genetics GENOMED Health Care Center in Poland.

MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1, COL3A1
Specificity
12 %
Genes
10 %
Marfan syndrome, TGFBR2.

By GGA - Galil Genetic Analysis in Israel.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz Syndrome, type 1B and 2B (TGFBR2).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
HAD panel 1.

By Connective Tissue Laboratory Ghent University Hospital in Belgium.

TGFB3, MYH11, ACTA2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1, COL3A1
Specificity
10 %
Genes
10 %
Standard Loeys-Dietz syndrome.

By Health in Code in Spain.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Aortic Valvular Diseases Panel.

By Health in Code in Spain.

ADAMTSL4, PRKG1, NKX2-5, TGFB3, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, SMAD4, PTPN11, PLOD1 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
10 %
Aortic diseases Panel.

By Health in Code in Spain.

GATA5, ADAMTSL4, B3GAT3, PRKG1, NKX2-5, TGFB3, EFEMP2, KCNJ8, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, ZDHHC9 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz syndrome 1B.

By Praxis fuer Humangenetik Wien in Austria.

TGFBR2
Specificity
100 %
Genes
10 %
qGenEx Craniofacial Anomalies.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

UBB, PAX7, HOXA2, TSHZ1, EIF4A3, DLX4, TBX22, SUMO1, KDM1A, SMOC2, WDR72, NOG, ODAPH, MMP20, KLK4, NECTIN1, ENAM, LTBP3, LRP6, PAX9 , (...)

View the complete list with 116 more genes
Specificity
1 %
Genes
10 %
Loeys-Dietz syndrome 2B.

By MedGene in Slovakia.

TGFBR2
Specificity
100 %
Genes
10 %
Invitae Aortopathy Comprehensive Panel.

By Invitae in United States.

PRKG1, TGFB3, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, SMAD4, PLOD1, COL5A2, COL5A1 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
Invitae Loeys-Dietz Syndrome Panel.

By Invitae in United States.

TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
25 %
Genes
10 %
Loeys-Dietz syndrome: TGFBR2 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Craniosysostosis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

FREM1, IFT122, IL11RA, IFT43, EFNB1, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR, RAB23, WDR35, FGFR1, FGFR2, FGFR3, RECQL4
Specificity
6 %
Genes
10 %
NGS panel - Aortic or arterial dilatation / dissection.

By Genome Diagnostics VU University Medical Center in Netherlands.

SMAD2, PRKG1, SCARF2, TGFB3, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, SMAD4, PLOD1, FBN1, ELN , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Familial Aortopathy Full Gene Sequencing Panel.

By Integrated Genetics Westborough Integrated Genetics in United States.

MYH11, ACTA2, TGFBR2, TGFBR1, FBN1, COL3A1
Specificity
17 %
Genes
10 %
Marfan Syndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, MED12, FLNA, COL5A2, COL5A1, CBS, FBN1, COL3A1
Specificity
6 %
Genes
10 %
Loeys-Dietz syndrome type 1B.

By Bioarray in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Familial thoracic aortic aneurysm and aortic dissection.

By Bioarray in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Familial Thoracic Aortic Aneurysm NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

SMAD6, MYH11, ACTA2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
10 %
Genes
10 %
Marfan Syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Loeys-Dietz Syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Loeys-Dietz Syndrome Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Aortic Aneurysm, Familial Thoracic Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

TGFB3, MYH11, SLC2A10, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
10 %
Genes
10 %
FAMILIAL THORACIC AORTIC ANEURYSM AND AORTIC DISSECTION: NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

MFAP5, PRKG1, TGFB3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, COL5A2, COL5A1, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Loeys-Dietz Syndrome Type 2, Sequencing TGFBR2 Gene.

By Reference Laboratory Genetics in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz Syndrome Type 2, Deletions-Duplications (MLPA) TGFBR2 Gene.

By Reference Laboratory Genetics in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 10 Genes.

By Reference Laboratory Genetics in Spain.

MYH11, ACTA2, FBN2, TGFBR2, TGFBR1, SMAD3, COL5A1, FBN1, COL3A1
Specificity
12 %
Genes
10 %
Familial Aortic Diseases , Panel Massive Sequencing 8 Genes.

By Reference Laboratory Genetics in Spain.

ADAMTSL4, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, FBN1
Specificity
13 %
Genes
10 %
Loeys-Dietz Syndrome: gene deletion/duplication.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
25 %
Genes
10 %
Heritable Thoracic Aortic Disease: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MAT2A, MFAP5, PRKG1, TGFB3, MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1, COL3A1
Specificity
8 %
Genes
10 %
NGS Aortic Dysfunction or Dilation and Related Disorders Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, PLOD1, COL5A2, COL5A1, CBS, FBN1, ELN, COL3A1, COL1A1, FBLN5
Specificity
5 %
Genes
10 %
NGS Connective Tissue Disorders Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A1, PKD2 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz syndrome type 2B.

By Center for Human Genetics, Inc in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Thoracic Aortic Aneurysms and Aortic Dissections (TGFBR1/2).

By Center for Human Genetics, Inc in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Familial Aortic Aneurysms.

By Center for Human Genetics, Inc in United States.

PRKG1, MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
13 %
Genes
10 %
Connective Tissue Disorders 22-gene panel.

By Center for Human Genetics, Inc in United States.

NTM, TGFBR3, PRKG1, MYH11, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, COL11A2, COL11A1, FLNA, COL5A2, COL5A1, FBN1, COL3A1, COL1A2 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
Marfan Syndrome Type 2.

By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz Syndrome.

By Johns Hopkins DNA Diagnostic Laboratory Johns Hopkins Hospital in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Thoracic aortic aneurysms and aortic dissection - full panel.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

MYH11, SLC2A10, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FBN1, COL3A1
Specificity
10 %
Genes
10 %
Thoracic aortic aneurysms and aortic dissection - familial variant analysis.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

MYH11, SLC2A10, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FBN1, COL3A1
Specificity
10 %
Genes
10 %
Craniosynostosis.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

IFT122, IL11RA, IFT43, MASP1, ASXL1, EFNB1, ALX4, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR, RAB23, WDR35, FGFR1, FGFR2, FGFR3 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
Marfan Syndrome and Related Disorders Deletion/Duplication Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
TGFBR2 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Craniofacial Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

ALX3, CD96, TCF12, ERF, ZIC1, MEGF8, DPH1, CDC45, ALX1, IFT122, IL11RA, IFT43, EFNB1, ALX4, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
Craniofacial Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

ALX3, CD96, TCF12, ERF, ZIC1, MEGF8, DPH1, CDC45, ALX1, IFT122, IL11RA, IFT43, EFNB1, ALX4, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
TGFBR2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan/TAAD Sequencing Panel.

By GeneDx in United States.

MYH11, SLC2A10, ACTA2, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, MED12, FLNA, COL5A2, COL5A1, CBS, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Marfan Syndrome/TAAD Del/Dup Panel.

By GeneDx in United States.

MYH11, SLC2A10, ACTA2, FBN2, TGFBR2, TGFBR1, SMAD3, COL5A2, COL5A1, CBS, FBN1, COL3A1
Specificity
9 %
Genes
10 %
Craniosynostosis.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

TCF12, ERF, ZIC1, MEGF8, CDC45, FREM1, IFT122, IL11RA, IFT43, ASXL1, EFNB1, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR, RAB23 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
10 %
CustomNext: Cardio.

By Ambry Genetics in United States.

TBX20, GATA4, TMPO, TXNRD2, TBX5, PRKG1, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
10 %
TAADNext.

By Ambry Genetics in United States.

PRKG1, TGFB3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, FLNA, SMAD4, PLOD1, COL5A2, COL5A1, CBS , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
TGFBR2, SMAD3, TGFBR1, TGFB2. NextGeneDx. Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
25 %
Genes
10 %
Pneumothorax Seq Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

TGFBR2, TGFBR1, FLCN, FBN1, COL3A1
Specificity
20 %
Genes
10 %
Pneumothorax Del/ Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

TGFBR2, TGFBR1, FLCN, FBN1, COL3A1
Specificity
20 %
Genes
10 %
Connective Tissue Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SMAD6, GATA5, LOX, SMAD2, MAT2A, B3GAT3, MFAP5, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz syndrome (sequence analysis of TGFBR2 gene).

By CGC Genetics in Portugal.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan and Loeys-Dietz syndromes and aortic aneurysm (NGS panel for 10 genes).

By CGC Genetics in Portugal.

MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
10 %
Genes
10 %
Loeys-Dietz syndrome (sequence analysis of TGFBR1 and TGFBR2 genes).

By CGC Genetics in Portugal.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
TGFBR2-Related Loeys-Dietz Syndrome.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2-Related Thoracic Aortic Aneurysms and Aortic Dissections.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan Syndrome and Related Aortopathies Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

LOX, MAT2A, MFAP5, PRKG1, TGFB3, EFEMP2, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12, SMS , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
10 %
Ehlers-Danlos Syndromes Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ATP6V1E1, AEBP1, ATP6V1A, LZTS1, ATP6AP1, FLNB, DSE, CHST3, RIN2, TNFRSF1A, GGCX, B3GALT6, C1R, C1S, GORAB, B3GAT3, SPARC, COL12A1, EFEMP2, ZNF469 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Sudden Cardiac Arrest Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MYL3, MYL2, DSC2, CSRP3, ACTN2, JPH2, TNNT2, TPM1, JUP, DSG2, NEXN, MYH6, TNNI3, TNNC1, MYLK2, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1 , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz Syndrome via TGFBR2 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Familial Thoracic Aortic Aneurysm and Dissection (TAAD) Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

LOX, MAT2A, MFAP5, PRKG1, TGFB3, FOXE3, MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, SMAD4, FBN1, COL3A1
Specificity
6 %
Genes
10 %
Craniosynostosis Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

CYP26B1, SLC25A24, TCF12, ERF, ZIC1, MEGF8, CDC45, FREM1, IFT122, IL11RA, IFT43, EFNB1, WDR19, GLI3, SKI, TGFBR2, TGFBR1, TWIST1, MSX2, POR , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
10 %
Loeys-Dietz syndrome core Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome core Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Marfan syndrome, type I / II Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, FBN1
Specificity
50 %
Genes
10 %
Loeys-Dietz syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

BGN, LOX, SMAD2, MAT2A, MFAP5, PRKG1, TGFB3, FOXE3, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, MED12 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2, FBN1
Specificity
17 %
Genes
10 %
Marfan syndrome and Loeys-Dietz syndrome core Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1, FBN1
Specificity
34 %
Genes
10 %
Loeys-Dietz syndrome core NGS panel.

By Connective Tissue Gene Tests in United States.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Loeys-Dietz syndrome 2 Sequencing test.

By Connective Tissue Gene Tests in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome 2 Comprehensive test.

By Connective Tissue Gene Tests in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome, type 1B and 2B.

By Institute of Human Genetics Cologne University in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Vascular and connective tissue diseases - panels.

By MGZ Medical Genetics Center in Germany.

JAM3, AIMP1, CST3, COL4A2, ADAMTSL4, ADA2, MAT2A, MFAP5, PRKG1, ADAR, ADCY6, TGFB3, BMPR2, EFEMP2, SMAD9, CAV1, KCNK3, BMPR1B, ACVRL1, ZNF469 , (...)

View the complete list with 47 more genes
Specificity
2 %
Genes
10 %
Teenager Stroke / Stroke-Like Episodes.

By MGZ Medical Genetics Center in Germany.

COL4A2, ADA2, ABCC6, SLC2A10, TGFBR2, TGFBR1, TGFB2, CACNA1C, HTRA1, TREX1, FLNA, COL4A1, NOTCH3, GLA, CBS, OTC, FBN1, POLG, AMACR, COL3A1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Loeys-Dietz syndrome.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Loeys-Dietz syndrome type 2B.

By Centogene AG - the Rare Disease Company in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Esophageal cancer, somatic.

By Centogene AG - the Rare Disease Company in Germany.

TGFBR2
Specificity
100 %
Genes
10 %
Connective tissue disorders - Ehlers-Danlos syndrome, Marfan syndrome, Loeys-Dietz syndrome, Aortic Aneurysm.

By CeGaT GmbH in Germany.

DSE, RIN2, B3GALT6, MAT2A, GORAB, MFAP5, PRKG1, TGFB3, LTBP4, EFEMP2, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
10 %
Familial Thoracic Aortic Aneurysm and Dissection and Related Syndromes.

By Asper Biogene Asper Biogene LLC in Estonia.

MYH11, SLC2A10, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, COL5A1, FBN1, COL3A1
Specificity
10 %
Genes
10 %
TGFBR2 mutational analysis.

By Connective Tissue Laboratory Ghent University Hospital in Belgium.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome, TGFBR2 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2 gene sequencing.

By Health in Code in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome 2B.

By Praxis fuer Humangenetik Wien in Austria.

TGFBR2
Specificity
100 %
Genes
10 %
Loeys-Dietz syndrome 1B.

By MedGene in Slovakia.

TGFBR2
Specificity
100 %
Genes
10 %
AORTOPATHIES, FAMILIAL.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

ADAMTSL4, TGFBR3, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, FBN1
Specificity
12 %
Genes
10 %
Marfan syndrome and related disorders.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MYH11, ACTA2, FBN2, TGFBR2, TGFBR1, SMAD3, TGFB2, COL5A2, COL5A1, FBN1, COL3A1
Specificity
10 %
Genes
10 %
NGS panel- Aortic or arterial dilatation/dissection.

By Genome Diagnostics VU University Medical Center in Netherlands.

SMAD2, PRKG1, SCARF2, TGFB3, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, SMAD4, PLOD1, FBN1, ELN , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
NGS panel- Aortic or arterial dilatation/dissection + COL5A1 + FLNA.

By Genome Diagnostics VU University Medical Center in Netherlands.

SMAD2, PRKG1, SCARF2, TGFB3, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, FLNA, SMAD4, PLOD1, COL5A1 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
10 %
NGS panel- Aortic or arterial dilatation/dissection + COL5A1.

By Genome Diagnostics VU University Medical Center in Netherlands.

SMAD2, PRKG1, SCARF2, TGFB3, EFEMP2, MYH11, SLC2A10, ACTA2, FBN2, MYLK, SKI, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2, SMAD4, PLOD1, COL5A1, FBN1 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
10 %
Marfan Syndrome, Thoracic Aortic Aneurysm & Dissection (TAAD), and Related Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MYH11, SLC2A10, ACTA2, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, MED12, FLNA, COL5A2, COL5A1, CBS, FBN1, COL3A1
Specificity
7 %
Genes
10 %
Connective Tissue Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
Connective Tissue Disorders: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

ACVR1, ZNF469, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, PKD2, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
Connective Tissue NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

ACVR1, ZNF469, ABCC6, CHST14, PRDM5, FKBP14, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, COL11A1, COL4A1, PKD2, ADAMTS2, PLOD1, COL5A2 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
10 %
Sudden Death Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

LRP6, CALR3, GJA5, NPPA, TMPO, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, RBM20, MYOZ2, JPH2, TNNT2, TPM1, JUP, DSG2, NEXN , (...)

View the complete list with 48 more genes
Specificity
2 %
Genes
10 %
TGFBR2.

By Fulgent Genetics Fulgent Genetics in United States.

TGFBR2
Specificity
100 %
Genes
10 %
Marfan Syndrome Panel.

By Blueprint Genetics in Finland.

ADAMTS17, VCAN, SMAD6, ADAMTS10, ADAMTSL4, ABL1, BGN, MAT2A, TGFB3, EFEMP2, SLC2A10, FBN2, SKI, TGFBR2, TGFBR1, SMAD3, TGFB2, UPF3B, MED12, COL11A2 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
10 %
Aorta Panel.

By Blueprint Genetics in Finland.

ADAMTS17, SMAD6, ADAMTS10, GATA5, ADAMTSL4, ENPP1, ABL1, BGN, SMAD2, MAT2A, MFAP5, TGFB3, EFEMP2, ZNF469, ABCC6, FKBP14, MYH11, SLC2A10, ACTA2, FBN2 , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
10 %
Ehlers-Danlos Syndrome Panel.

By Blueprint Genetics in Finland.

DSE, BGN, EFEMP2, ZNF469, ABCC6, CHST14, FKBP14, FBN2, TGFBR2, TGFBR1, SMAD3, TGFB2, COL11A1, FLNA, ADAMTS2, PLOD1, COL5A2, COL5A1, CBS, SLC39A13 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
10 %
Craniosynostosis Panel.

By Blueprint Genetics in Finland.

NOG, TWIST2, GDF5, FLNB, ALX3, TCF12, ERF, ZIC1, MEGF8, CDC45, ESCO2, BMP4, FREM1, IFT122, IL11RA, MASP1, EFNB1, ALX4, WDR19, IFT140 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
10 %
Marfan syndrome type 2.

By Bioarray in Spain.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

TGFBR2
Specificity
100 %
Genes
10 %
TGFBR2 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

TGFBR2
Specificity
100 %
Genes
10 %
Collagenopathies.

By Cardiovascular Genetics PO San Francesco-NUORO (IT) in Italy.

TGFBR2, TGFBR1, SMAD3, COL5A1, FBN1, ELN, TGFB1
Specificity
15 %
Genes
10 %
FAMILIAL THORACIC AORTIC ANEURYSM AND AORTIC DISSECTION.

By Laboratorio de Genetica Clinica SL in Spain.

MYH11, ACTA2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
15 %
Genes
10 %
MARFAN SYNDROME TYPE 2/ LOEYS-DIETZ SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

TGFBR2, TGFBR1
Specificity
50 %
Genes
10 %
Aortic aneurysm, hereditary thoracic panel.

By LifeLabs Genetics in Canada.

MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, TGFB2, CBS, FBN1, COL3A1
Specificity
9 %
Genes
10 %
Loeys-Dietz Syndrome , Panel Massive Sequencing (NGS) 5 Genes.

By Reference Laboratory Genetics in Spain.

TGFB3, TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
20 %
Genes
10 %
Conective Tissue Related Disorders , Panel Massive Sequencing (NGS) 39 Genes.

By Reference Laboratory Genetics in Spain.

ADAMTS10, TGFB3, EFEMP2, ACVR1, ZNF469, ABCC6, CHST14, TNXB, PRDM5, FKBP14, MYH11, SLC2A10, ACTA2, FBN2, MYLK, TGFBR2, TGFBR1, SMAD3, NOTCH1, TGFB2 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
10 %
Loeys-Dietz Syndrome: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

TGFBR2, TGFBR1, SMAD3, TGFB2
Specificity
25 %
Genes
10 %
HNPCC MSI & IHC Screening.

By Baylor Miraca Genetics Laboratories in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
PMS2 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

PMS2
Specificity
100 %
Genes
10 %
PMS2 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

PMS2
Specificity
100 %
Genes
10 %
PMS2 Sequence Analysis.

By Baylor Miraca Genetics Laboratories in United States.

PMS2
Specificity
100 %
Genes
10 %
PMS2 Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories in United States.

PMS2
Specificity
100 %
Genes
10 %
Mismatch Repair Proteins Immunohistochemistry.

By Baylor Miraca Genetics Laboratories in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Hereditary Brain, CNS, PNS Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, MRE11, ATM, ALK, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
24 %
Genes
37 %
High Risk Hereditary Colorectal Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

SMAD4, BMPR1A, STK11, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
42 %
Genes
46 %
Turcot syndrome.

By Center for Human Genetics, Inc in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Hereditary Non-Polyposis Colon Cancer.

By Center for Human Genetics, Inc in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Comprehensive breast and ovarian cancer panel testing (18 genes).

By Molecular Genetics Laboratory North York General Hospital in Canada.

RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
28 %
Genes
46 %
PMS2 sequence analysis.

By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center in United States.

PMS2
Specificity
100 %
Genes
10 %
Inherited Cancer Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

CDKN1B, BAP1, XRCC2, MITF, NF1, RAD51D, BARD1, RAD51C, CDC73, PRKAR1A, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, MET, FLCN, CDKN2A, CDK4 , (...)

View the complete list with 29 more genes
Specificity
11 %
Genes
46 %
Inherited Colon Cancer.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

GREM1, POLD1, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
56 %
Genes
46 %
Hereditary Nonpolyposis Colorectal Cander (HNPCC): PMS2 (Known Mutation).

By Molecular Diagnostic Laboratory LabCorp in United States.

PMS2
Specificity
100 %
Genes
10 %
PMS2 Deletion/Duplication Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

PMS2
Specificity
100 %
Genes
10 %
VistaSeq Hereditary Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

ABRAXAS1, RAD51D, BARD1, RAD51C, PRKAR1A, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MUTYH, MLH1 , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
Vistaseq Hereditary Cancer Panel Without BRCA.

By Molecular Diagnostic Laboratory LabCorp in United States.

ABRAXAS1, RAD51D, BARD1, RAD51C, PRKAR1A, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MUTYH, MLH1 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
VistaSeq Brain/CNS/PNS Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

SMARCB1, NF1, SUFU, NF2, PHOX2B, PTCH1, NBN, ALK, MEN1, RB1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
24 %
Genes
37 %
VistaSeq High Risk Colorectal Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
72 %
Genes
46 %
VistaSeq Renal Cell Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

MITF, GPC3, MET, FLCN, SDHD, TSC1, TSC2, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, VHL
Specificity
27 %
Genes
46 %
VistaSeq GYN Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

CHEK2, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
46 %
Genes
46 %
Tier 1: Hereditary Lymphoma and Immunodeficiency Panel.

By Genetic Services Laboratory University of Chicago in United States.

NPAT, POT1, TERF2IP, KLHDC8B, ACD, CHEK2, TP53, MLH1, MSH6, PMS2, MSH2
Specificity
37 %
Genes
37 %
Hereditary Gastric Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

PDGFRA, KIT, CTNNA1, SMAD4, BMPR1A, STK11, CDH1, SDHB, SDHC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
27 %
Genes
46 %
Comprehensive Hereditary Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

DDX41, SAMD9L, SAMD9, POLE, ETV6, IKZF1, POLD1, SRP72, BAP1, TERT, TERC, NF1, RTEL1, CEBPA, PAX5, GATA2, BRIP1, SMAD4, BMPR1A, MAX , (...)

View the complete list with 34 more genes
Specificity
10 %
Genes
46 %
Hereditary Myeloid Malignancy and Inherited Bone Marrow Failure Panel.

By Genetic Services Laboratory University of Chicago in United States.

RAD51, UBE2T, SAMD9L, SAMD9, NAF1, POT1, DNAJC21, ACD, CXCR4, GFI1, RBM8A, RPL26, VPS45, G6PC3, RPL15, ELANE, CSF3R, ETV6, IKZF1, USB1 , (...)

View the complete list with 59 more genes
Specificity
6 %
Genes
37 %
Comprehensive Hereditary Breast/Ovarian Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

RAD51D, BARD1, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
28 %
Genes
46 %
Hereditary nonpolyposis colon cancer.

By Institute of Human Genetics Universitätsmedizin Greifswald in Germany.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
PMS2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

PMS2
Specificity
100 %
Genes
10 %
PMS2.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Cancer Panel - High Penetrance 16.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
32 %
Genes
46 %
HNPCC/Lynch Syndrome (PMS2) Sequencing and Deletion/Duplication.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

PMS2
Specificity
100 %
Genes
10 %
HNPCC/Lynch Syndrome Del/Dup.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Comprehensive Cancer Panel.

By GeneDx in United States.

AXIN2, XRCC2, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, FANCC, TP53, PTEN, MUTYH , (...)

View the complete list with 9 more genes
Specificity
18 %
Genes
46 %
Oncology High/Moderate Risk Panel.

By GeneDx in United States.

RAD51D, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC , (...)

View the complete list with 3 more genes
Specificity
22 %
Genes
46 %
Breast/Ovarian Cancer Panel.

By GeneDx in United States.

XRCC2, RAD51D, BARD1, RAD51C, BRIP1, CHEK2, CDH1, PALB2, NBN, ATM, FANCC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
25 %
Genes
46 %
Colorectal Cancer Panel.

By GeneDx in United States.

AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
27 %
Genes
46 %
Endometrial Cancer Panel.

By GeneDx in United States.

POLD1, CHEK2, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
42 %
Genes
46 %
Renal Cancer Panel.

By GeneDx in United States.

BAP1, MITF, MET, FLCN, SDHD, TSC1, TSC2, SDHB, FH, SDHC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, VHL
Specificity
28 %
Genes
46 %
Hereditary Cancer Panel - Breast/Ovarian/Uterine26.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

ABRAXAS1, XRCC2, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, FANCC, TP53, PTEN, MUTYH, MLH1 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
46 %
Hereditary Cancer Panel - Renal19.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

MITF, CDC73, MET, FLCN, SDHD, TSC1, TSC2, SDHA, SDHB, FH, SDHC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, VHL
Specificity
27 %
Genes
46 %
Hereditary Cancer Panel - Neuro17.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

NF1, SUFU, NF2, PHOX2B, PTCH1, NBN, ALK, TSC1, TSC2, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
24 %
Genes
37 %
Hereditary Cancer Panel - Pancreatic14.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
36 %
Genes
46 %
Hereditary Cancer Panel - Colorectal20.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

GALNT12, AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
25 %
Genes
46 %
Hereditary Cancer Panel - Breast/Ovarian17.

By Human Genetics Laboratory, Munroe-Meyer Institute University of Nebraska Medical Center in United States.

RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
30 %
Genes
46 %
BrainTumorNext.

By Ambry Genetics in United States.

DICER1, POT1, AIP, CDKN1B, SMARCB1, SMARCA4, SMARCE1, NF1, PRKAR1A, CDKN2A, SUFU, NF2, PHOX2B, PTCH1, NBN, ALK, TSC1, TSC2, MEN1, TP53 , (...)

View the complete list with 7 more genes
Specificity
15 %
Genes
37 %
CancerNext.

By Ambry Genetics in United States.

HOXB13, DICER1, POLE, GREM1, POLD1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2 , (...)

View the complete list with 14 more genes
Specificity
15 %
Genes
46 %
CustomNext: Cancer.

By Ambry Genetics in United States.

NTHL1, HOXB13, GALNT12, DICER1, POT1, AIP, POLE, GREM1, POLD1, CDKN1B, BAP1, XRCC2, SMARCB1, SMARCA4, SMARCE1, MITF, NF1, RAD51D, BARD1, RAD51C , (...)

View the complete list with 48 more genes
Specificity
8 %
Genes
46 %
OvaNext.

By Ambry Genetics in United States.

DICER1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
ProstateNext.

By Ambry Genetics in United States.

HOXB13, RAD51D, CHEK2, PALB2, NBN, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
36 %
Genes
46 %
PancNext.

By Ambry Genetics in United States.

CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
39 %
Genes
46 %
RenalNext.

By Ambry Genetics in United States.

BAP1, MET, FLCN, SDHD, TSC1, TSC2, SDHA, SDHB, FH, SDHC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, VHL
Specificity
28 %
Genes
46 %
TumorNext-HRD+CancerNext.

By Ambry Genetics in United States.

HOXB13, DICER1, POLE, GREM1, POLD1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2 , (...)

View the complete list with 14 more genes
Specificity
15 %
Genes
46 %
TumorNext-HRD+OvaNext.

By Ambry Genetics in United States.

DICER1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
HNPCC/Lynch Syndrome Panel.

By Ambry Genetics in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
MLH1, MSH2, MSH6 gene sequence and deletion/duplication and EPCAM deletion/duplication reflex to PMS2 gene sequence and deletion/duplication.

By Ambry Genetics in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
PMS2 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Breast, Ovarian, and Endometrial Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

WRN, ITK, FANCA, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, ATM, MEN1, TP53, PTEN, MUTYH , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
Hereditary Pancreatic Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

PRSS1, SMAD4, BMPR1A, CDKN2A, CDK4, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
28 %
Genes
46 %
Hereditary Brain Tumor Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SMARCB1, SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, ATM, ALK, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
24 %
Genes
37 %
Hereditary nonpolyposis colorectal cancer (HNPCC, deletion/duplication analysis on PMS2 gene).

By CGC Genetics in Portugal.

PMS2
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer (HNPCC, sequence analysis of PMS2 gene).

By CGC Genetics in Portugal.

PMS2
Specificity
100 %
Genes
10 %
MLH1/MSH2/MSH6/PMS2/EPCAM Somatic Tumor MMR Sequencing and Deletion/Duplication Test.

By Impact Genetics Impact Genetics in Canada.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Colorectal Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

POLE, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
30 %
Genes
46 %
Pancreatic Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

PALLD, CDKN2A, CDK4, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
32 %
Genes
46 %
Lynch Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Hereditary Endometrial Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

POLD1, CHEK2, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
42 %
Genes
46 %
Hereditary Breast and Ovarian Cancer - Expanded and Lynch Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DICER1, XRCC2, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, FANCC, TP53, PTEN, MUTYH , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
Prostate Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

HOXB13, RAD51D, RAD51C, BRIP1, CHEK2, PALB2, NBN, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
32 %
Genes
46 %
Lynch Syndrome gene sequencing and deletion/dupliction analysis.

By Molecular Diagnostics Laboratory University Health Network in Canada.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
PMS2-Related Lynch Syndrome.

By MGZ Medical Genetics Center in Germany.

PMS2
Specificity
100 %
Genes
10 %
Ovarian Cancer – Basic Diagnostics.

By MGZ Medical Genetics Center in Germany.

RAD51D, RAD51C, BRIP1, CHEK2, PALB2, NBN, TP53, MLH1, MSH6, PMS2, MSH2, BRCA2, BRCA1
Specificity
31 %
Genes
37 %
Breast Cancer.

By MGZ Medical Genetics Center in Germany.

CEP57, BUB1B, FANCD2, FANCI, FANCL, FANCM, SLX4, FANCE, FANCF, FANCG, FANCA, FANCB, NF1, RAD51D, RAD51C, BRIP1, CHEK2, SDHD, STK11, CDH1 , (...)

View the complete list with 17 more genes
Specificity
11 %
Genes
37 %
CentoColon extended panel.

By Centogene AG - the Rare Disease Company in Germany.

NTHL1, POLE, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
30 %
Genes
46 %
Colorectal cancer, hereditary nonpolyposis type 4.

By Centogene AG - the Rare Disease Company in Germany.

PMS2
Specificity
100 %
Genes
10 %
Renal cell carcinoma Panel.

By CeGaT GmbH in Germany.

BAP1, MITF, MET, FLCN, SDHD, PALB2, TSC1, TSC2, SDHA, SDHB, FH, SDHC, HNF1B, SDHAF2, WT1, HNF1A, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
Syndromes with immunodeficiency Panel.

By CeGaT GmbH in Germany.

SP110, RPSA, FCGR3A, ZBTB24, MCM4, SPINK5, RNF168, DNMT3B, TYK2, SMARCAL1, PDGFRA, NOD2, NHP2, CFH, FGF10, ADAR, DOCK8, TERT, TERC, DKC1 , (...)

View the complete list with 18 more genes
Specificity
3 %
Genes
10 %
Lynch Syndrome, Colorectal Cancer, PMS2.

By GGA - Galil Genetic Analysis in Israel.

PMS2
Specificity
100 %
Genes
10 %
Lynch syndrome/HNPCC (MLH1, MSH2, MSH6, PMS2, EPCAM).

By Center for Human Genetics Cliniques Universitaires Saint Luc in Belgium.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Inherited Cancer Screen.

By Counsyl in United States.

POLE, GREM1, POLD1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, MRE11, ATM, SDHA , (...)

View the complete list with 16 more genes
Specificity
14 %
Genes
46 %
qCancer Risk.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

POLE, POLD1, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53 , (...)

View the complete list with 10 more genes
Specificity
17 %
Genes
46 %
qCancer Risk Expanded.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

POLE, POLD1, MITF, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, MET, FLCN, SDHD, CDKN2A, CDK4, STK11, CDH1 , (...)

View the complete list with 25 more genes
Specificity
12 %
Genes
46 %
qCancer Gine.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

POLD1, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
qCancer Colorrectal.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
30 %
Genes
46 %
Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI).

By Invitae in United States.

DICER1, AXIN2, POLE, PDGFRA, GREM1, POLD1, KIT, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, SDHD, CDKN2A, STK11 , (...)

View the complete list with 22 more genes
Specificity
12 %
Genes
46 %
Invitae Gastric Cancer Panel.

By Invitae in United States.

PDGFRA, KIT, NF1, SMAD4, BMPR1A, SDHD, STK11, CDH1, SDHA, SDHB, SDHC, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
28 %
Genes
46 %
Invitae Multi-Cancer Panel.

By Invitae in United States.

DIS3L2, HOXB13, DICER1, WRN, POT1, AXIN2, POLE, PDGFRA, EGFR, GREM1, POLD1, CDKN1B, BAP1, KIT, SMARCB1, SMARCA4, SMARCE1, TERT, TERC, MITF , (...)

View the complete list with 60 more genes
Specificity
7 %
Genes
46 %
Invitae Breast and Gyn Cancers Guidelines-Based Panel.

By Invitae in United States.

NF1, RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
27 %
Genes
46 %
Invitae Pediatric Nervous System/Brain Tumors Panel.

By Invitae in United States.

DICER1, SMARCB1, SMARCE1, NF1, PRKAR1A, SUFU, NF2, PHOX2B, PTCH1, ALK, TSC1, TSC2, HRAS, MEN1, RB1, TP53, PTEN, MLH1, MSH6, PMS2 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
Invitae Pediatric Hematologic Malignancies Panel.

By Invitae in United States.

TERT, TERC, NF1, CEBPA, GATA2, NBN, ATM, HRAS, BLM, TP53, RUNX1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
32 %
Genes
46 %
Invitae Myelodysplastic Syndrome/Leukemia Panel.

By Invitae in United States.

TERT, TERC, NF1, CEBPA, GATA2, NBN, ATM, HRAS, BLM, TP53, RUNX1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
32 %
Genes
46 %
Invitae Lynch Syndrome Panel.

By Invitae in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Invitae Pancreatic Cancer Panel.

By Invitae in United States.

NF1, SMAD4, BMPR1A, CDKN2A, STK11, PALB2, ATM, TSC1, TSC2, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
25 %
Genes
46 %
Invitae Breast and Gyn Cancers Panel.

By Invitae in United States.

DICER1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2 , (...)

View the complete list with 3 more genes
Specificity
22 %
Genes
46 %
Invitae Colorectal Cancer Guidelines-Based Panel.

By Invitae in United States.

SMAD4, BMPR1A, STK11, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
42 %
Genes
46 %
Invitae Primary Immunodeficiency Panel.

By Invitae in United States.

IRF7, RORC, DCLRE1B, DOCK2, MAP3K14, NFAT5, IL17RC, TAPBP, TAP2, TNFRSF4, RHOH, FPR1, SP110, TNFSF12, IKBKB, LCK, CTPS1, ZBTB24, ADAM17, BCL10 , (...)

View the complete list with 187 more genes
Specificity
1 %
Genes
10 %
Lynch Syndrome: PMS2 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Cancer Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

BUB1B, AIP, POLD1, CDKN1B, BAP1, XRCC2, MGMT, SMARCB1, SMARCA4, RAD51D, BARD1, RAD51C, CDC73, PRKAR1A, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2 , (...)

View the complete list with 40 more genes
Specificity
7 %
Genes
37 %
Brain, CNS, and PNS Cancer: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, ATM, ALK, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
25 %
Genes
37 %
Breast and Ovarian Cancer: Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

XRCC2, SMARCA4, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
Gastrointestinal and Colorectal Cancer: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

POLD1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC, BRCA2, BRCA1
Specificity
22 %
Genes
37 %
Lynch Syndrome (HNPCC) Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Pancreatic Cancer NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

BAP1, CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
36 %
Genes
46 %
PMS2.

By Fulgent Genetics Fulgent Genetics in United States.

PMS2
Specificity
100 %
Genes
10 %
Focus Cancer Panel - 40 Genes.

By Fulgent Genetics Fulgent Genetics in United States.

RAD51, AXIN2, POLE, BAP1, KIT, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, MET, CDKN2A, CDK4, STK11, CDH1, PALB2 , (...)

View the complete list with 20 more genes
Specificity
13 %
Genes
46 %
Endometrial Cancer Focus Panel.

By Fulgent Genetics Fulgent Genetics in United States.

POLD1, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
50 %
Genes
46 %
Ovarian Cancer Focus Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RAD51D, BARD1, RAD51C, BRIP1, STK11, NBN, MRE11, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
32 %
Genes
46 %
Nervous System / Brain Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

DICER1, SMARCB1, SMARCA4, SMARCE1, NF1, PRKAR1A, SUFU, NF2, PHOX2B, PTCH1, ATM, ALK, TSC1, TSC2, HRAS, MEN1, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Pancreatic Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

NF1, SMAD4, BMPR1A, CDKN2A, CDK4, STK11, PALB2, ATM, TSC1, TSC2, FANCC, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL , (...)

View the complete list with 2 more genes
Specificity
23 %
Genes
46 %
Ovarian Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SMARCA4, RAD51D, BARD1, RAD51C, BRIP1, STK11, NBN, MRE11, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
30 %
Genes
46 %
Prostate Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

HOXB13, CHEK2, NBN, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
46 %
Genes
46 %
Sarcoma Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

DICER1, WRN, PDGFRA, KIT, NF1, PRKAR1A, SDHD, CDKN1C, SUFU, PTCH1, NBN, HRAS, BLM, SDHA, SDHB, FH, SDHC, RB1, TP53, RECQL4 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
46 %
Renal / Urinary Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

DIS3L2, DICER1, BAP1, SMARCB1, SMARCA4, MITF, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, TSC1, TSC2, SDHA, SDHB, FH, SDHC, WT1, TP53 , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
MyVantage(TM) Hereditary Comprehensive Cancer Panel.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

POLE, POLD1, NF1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, SDHD, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, MEN1, SDHB , (...)

View the complete list with 14 more genes
Specificity
15 %
Genes
46 %
Lynch Syndrome Panel.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Severe Combined Immunodeficiency Panel.

By Blueprint Genetics in Finland.

BCL11B, TFRC, POLE2, LAT, MSN, NSMCE3, MAP3K14, TAPBP, TAP2, TNFRSF4, RHOH, SP110, IKBKB, LCK, IRF8, CD247, CD8A, STAT2, CORO1A, CD3G , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
10 %
Hereditary Colorectal Cancer Panel.

By Blueprint Genetics in Finland.

NTHL1, AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, STK11, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
28 %
Genes
46 %
Hereditary Pancreatic Cancer Panel.

By Blueprint Genetics in Finland.

BUB1B, NF1, SMAD4, BMPR1A, CDKN2A, STK11, PALB2, ATM, TSC1, TSC2, FANCC, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL , (...)

View the complete list with 2 more genes
Specificity
23 %
Genes
46 %
Hereditary Gastrointestinal Cancer Panel.

By Blueprint Genetics in Finland.

NTHL1, RHBDF2, BUB1B, AXIN2, POLE, PDGFRA, GREM1, POLD1, KIT, SMARCB1, NF1, SMAD4, BMPR1A, SDHD, CDKN2A, STK11, CDH1, PALB2, ATM, TSC1 , (...)

View the complete list with 19 more genes
Specificity
13 %
Genes
46 %
Hereditary Breast and Gynecological Cancer Panel.

By Blueprint Genetics in Finland.

DICER1, XRCC2, FANCM, SMARCA4, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, BLM, TP53, PTEN , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
Mismatch repair cancer syndrome.

By Bioarray in Spain.

PMS2
Specificity
100 %
Genes
10 %
Lynch syndrome type IV.

By Bioarray in Spain.

PMS2
Specificity
100 %
Genes
10 %
iGene Cancer Panel.

By ApolloGen, Inc. in United States.

NF1, RAD51C, BRIP1, SMAD4, BMPR1A, CDKN2A, STK11, CDH1, PALB2, PTCH1, NBN, ATM, MEN1, RET, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2 , (...)

View the complete list with 5 more genes
Specificity
16 %
Genes
37 %
Hereditary Colon and Endometrial Cancer-ColoNGS.

By GeneKor MSA in Greece.

MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
72 %
Genes
46 %
Hereditary Breast and Ovarian Cancer 26 Gene Panel.

By Veritas Genetics Veritas Genetics in United States.

ABRAXAS1, XRCC2, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, MEN1, TP53, PTEN, MUTYH, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Hereditary Colon Cancer , Panel Massive Sequencing (NGS) 14 Genes.

By Reference Laboratory Genetics in Spain.

MSH3, ENG, SMAD4, BMPR1A, FLCN, STK11, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
36 %
Genes
46 %
Breast and Ovarian Hereditary Cancer , Panel Massive Sequencing (NGS) 20 Genes.

By Reference Laboratory Genetics in Spain.

NF1, RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
25 %
Genes
46 %
Hereditary Renal Cancer , Panel Massive Sequencing (NGS) 21 Genes.

By Reference Laboratory Genetics in Spain.

DIS3L2, BAP1, MITF, MET, FLCN, SDHD, TSC1, TSC2, SDHB, FH, HNF1B, WT1, HNF1A, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 1 more genes
Specificity
24 %
Genes
46 %
Uterine Cancer , Panel Massive Sequencing (NGS) 6 Genes.

By Reference Laboratory Genetics in Spain.

PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
84 %
Genes
46 %
Hereditary Sarcoma (Susceptibility to) , Panel Massive Sequencing (NGS) 25 Genes.

By Reference Laboratory Genetics in Spain.

DICER1, WRN, KIT, NF1, PRKAR1A, SDHD, CDKN1C, SUFU, PTCH1, NBN, HRAS, BLM, SDHB, FH, SDHC, SDHAF2, RB1, TP53, RECQL4, MLH1 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
genTrue.

By True Health Diagnostics in United States.

POLE, POLD1, RAD51D, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MUTYH, MLH1, MSH6 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
46 %
Phosphorus Colorectal Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
28 %
Genes
46 %
Phosphorus Leukemia including Fanconi Anemia Genes Panel.

By Phosphorus Diagnostics LLC in United States.

ERCC4, XRCC2, FANCD2, FANCI, FANCL, FANCM, SLX4, FANCE, FANCF, FANCG, FANCA, TERT, TERC, DKC1, FANCB, NF1, RAD51C, CEBPA, GATA2, BRIP1 , (...)

View the complete list with 15 more genes
Specificity
15 %
Genes
46 %
Phosphorus Prostate Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

HOXB13, RAD51D, CHEK2, NBN, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
39 %
Genes
46 %
Brain, CNS, and PNS Cancer: Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, ATM, ALK, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
25 %
Genes
37 %
Breast and Ovarian Cancer: Sequencing and Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

XRCC2, SMARCA4, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
Gastrointestinal and Colorectal Cancer: gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

POLD1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC, BRCA2, BRCA1
Specificity
22 %
Genes
37 %
Lynch Syndrome: Microsatellite Instability.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Lynch Syndrome: MLH1, MSH2, MSH6, and PMS2 Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Hereditary Cancer Syndrome: Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BUB1B, AIP, POLD1, CDKN1B, BAP1, XRCC2, MGMT, SMARCB1, SMARCA4, RAD51D, BARD1, RAD51C, CDC73, PRKAR1A, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2 , (...)

View the complete list with 40 more genes
Specificity
7 %
Genes
37 %
Hereditary Brain, CNS, PNS Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, MRE11, ATM, ALK, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL
Specificity
24 %
Genes
37 %
Hereditary Pancreatic Cancer Panel.

By Baylor Miraca Genetics Laboratories in United States.

RAD50, SMAD4, BMPR1A, CDKN2A, CDK4, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
30 %
Genes
46 %
Lynch syndrome/HNPCC (MLH1, MSH2, MSH6, PMS2, TACSTD1).

By Center for Human Genetics, Inc in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Lynch syndrome (MLH1, MSH2, MSH6, PMS2, EPCAM) Mutation, Deletion/Duplication Analysis.

By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Inherited Ovarian Cancer.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
72 %
Genes
46 %
MLH1/MSH2/MSH6/PMS2 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
PMS2 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

PMS2
Specificity
100 %
Genes
10 %
VisaSeq Breast and GYN Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

ABRAXAS1, NF1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, FANCC, TP53, PTEN, MUTYH, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
VistaSeq Pancreatic Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
36 %
Genes
46 %
VistaSeq Colorectal Cancer Panel.

By Molecular Diagnostic Laboratory LabCorp in United States.

AXIN2, POLE, POLD1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC , (...)

View the complete list with 2 more genes
Specificity
23 %
Genes
46 %
myRisk Hereditary Cancer.

By Myriad Genetic Laboratories, Inc. Myriad Genetic Laboratories, Inc. in United States.

POLE, GREM1, POLD1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MUTYH , (...)

View the complete list with 8 more genes
Specificity
18 %
Genes
46 %
COLARIS Plus.

By Myriad Genetic Laboratories, Inc. Myriad Genetic Laboratories, Inc. in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Tier 2: Familial Myelodysplastic Syndrome/Acute Leukemia (MDS/AL) Panel.

By Genetic Services Laboratory University of Chicago in United States.

NF1, CHEK2, ATM, CBL, PTPN11, BLM, TP53, MLH1, MSH6, PMS2, MSH2, BRCA2, BRCA1
Specificity
31 %
Genes
37 %
Lynch Syndrome Panel.

By Genetic Services Laboratory University of Chicago in United States.

POLE, POLD1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
72 %
Genes
46 %
Hereditary Leukemia and Breast Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

DDX41, SAMD9L, SAMD9, ETV6, IKZF1, SRP72, TERT, TERC, NF1, RTEL1, CEBPA, PAX5, GATA2, CHEK2, CDH1, PALB2, NBN, ATM, CBL, PTPN11 , (...)

View the complete list with 11 more genes
Specificity
13 %
Genes
37 %
Hereditary Colorectal Cancer High Risk Panel.

By Genetic Services Laboratory University of Chicago in United States.

POLE, POLD1, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
56 %
Genes
46 %
Comprehensive Hereditary Colorectal Cancer Panel.

By Genetic Services Laboratory University of Chicago in United States.

GALNT12, BUB1B, AXIN2, POLE, GREM1, POLD1, ENG, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 1 more genes
Specificity
24 %
Genes
46 %
Hereditary Cancer Panel Comprehensive.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

POLE, GREM1, POLD1, CTNNA1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, SDHB, TP53 , (...)

View the complete list with 10 more genes
Specificity
17 %
Genes
46 %
Cancer Panel, Hereditary, Sequencing 46 Genes, Deletion/Duplication, 47 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

CDKN1B, BAP1, SMARCB1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, MAX, CHEK2, MET, FLCN, SDHD, CDKN2A, CDK4, STK11, CDH1, SUFU, PALB2 , (...)

View the complete list with 27 more genes
Specificity
11 %
Genes
46 %
Gastrointestinal Hereditary Cancer Panel, Sequencing and Deletion/Duplication, 16 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

SMAD4, BMPR1A, SDHD, STK11, CDH1, SDHB, SDHC, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
32 %
Genes
46 %
Lynch/Colorectal High Risk Panel.

By GeneDx in United States.

MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
72 %
Genes
46 %
Pancreatic Cancer Panel.

By GeneDx in United States.

XRCC2, CDKN2A, CDK4, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
32 %
Genes
46 %
OncoGeneDx Custom Panel.

By GeneDx in United States.

AXIN2, XRCC2, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, FANCC, TP53, PTEN, MUTYH , (...)

View the complete list with 9 more genes
Specificity
18 %
Genes
46 %
Lynch Syndrome.

By Molecular Diagnostic Laboratory University of Alberta in Canada.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
CancerNext-Expanded.

By Ambry Genetics in United States.

HOXB13, GALNT12, DICER1, POT1, POLE, GREM1, POLD1, CDKN1B, BAP1, XRCC2, SMARCB1, SMARCA4, SMARCE1, MITF, NF1, RAD51D, BARD1, RAD51C, PRKAR1A, BRIP1 , (...)

View the complete list with 44 more genes
Specificity
8 %
Genes
46 %
ColoNext.

By Ambry Genetics in United States.

POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
30 %
Genes
46 %
GYNplus.

By Ambry Genetics in United States.

RAD51D, RAD51C, BRIP1, PALB2, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
39 %
Genes
46 %
PMS2 gene sequence and deletion/duplication.

By Ambry Genetics in United States.

PMS2
Specificity
100 %
Genes
10 %
PMS2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Colorectal and Gastrointestinal Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

POLE, POLD1, KIT, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM , (...)

View the complete list with 3 more genes
Specificity
22 %
Genes
46 %
Hereditary High-Risk Colorectal Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SMAD4, BMPR1A, STK11, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
42 %
Genes
46 %
CHOP Comprehensive Hereditary Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

DDB2, DIS3L2, MTAP, CEBPE, POLH, ARID5B, HMBS, RHBDF2, CYLD, BUB1B, XPA, ERCC5, DICER1, DDX41, COL7A1, G6PC3, ITK, ELANE, EXT1, EXT2 , (...)

View the complete list with 86 more genes
Specificity
5 %
Genes
46 %
Hereditary nonpolyposis colorectal cancer (HNPCC, NGS panel for 5 genes).

By CGC Genetics in Portugal.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Breast cancer (NGS panel for 18 genes).

By CGC Genetics in Portugal.

ERCC4, RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, BRCA2, BRCA1
Specificity
23 %
Genes
37 %
OncoRisk (NGS panel for 48 genes).

By CGC Genetics in Portugal.

EXT1, EXT2, FANCA, FANCB, NF1, RAD51C, CDC73, PRKAR1A, CEBPA, BRIP1, SMAD4, BMPR1A, MAX, CHEK2, MET, FLCN, SDHD, CDKN1C, CDKN2A, CDK4 , (...)

View the complete list with 28 more genes
Specificity
11 %
Genes
46 %
OncoRisk Plus (NGS panel for 89 genes).

By CGC Genetics in Portugal.

CEP57, DDB2, DIS3L2, XPC, CYLD, BUB1B, XPA, ERCC5, DICER1, WRN, AIP, EXT1, EXT2, ERCC4, BAP1, FANCD2, FANCI, FANCL, FANCM, SLX4 , (...)

View the complete list with 69 more genes
Specificity
6 %
Genes
46 %
Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

POLE, POLD1, NF1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, MEN1, RET, TP53 , (...)

View the complete list with 11 more genes
Specificity
17 %
Genes
46 %
Renal Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DIS3L2, DICER1, BAP1, SMARCB1, MITF, CDC73, CHEK2, MET, FLCN, SDHD, TSC1, TSC2, SDHA, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Lynch Syndrome via PMS2 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Ovarian Cancer Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DICER1, SMARCA4, NF1, RAD51D, BARD1, RAD51C, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Hereditary Breast and Ovarian Cancer - High Risk and Lynch Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
30 %
Genes
46 %
Custom gene seqeuncing panel.

By Molecular Diagnostics Laboratory University Health Network in Canada.

LYZ, B2M, POT1, FGA, APOA1, BAP1, MITF, RYR1, CACNA1S, MET, FLCN, SDHD, CDKN2A, CDK4, TSC1, TSC2, SDHA, GSN, SDHB, FH , (...)

View the complete list with 10 more genes
Specificity
17 %
Genes
46 %
Hereditary Nonpolyposis Colon Cancer.

By MGZ Medical Genetics Center in Germany.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Ovarian Cancer.

By MGZ Medical Genetics Center in Germany.

CEP57, BUB1B, DICER1, FANCD2, FANCI, FANCL, SLX4, FANCE, FANCF, FANCG, FANCA, FANCB, RAD51D, RAD51C, BRIP1, CHEK2, PALB2, NBN, ATM, FANCC , (...)

View the complete list with 7 more genes
Specificity
15 %
Genes
37 %
CentoCancer panel.

By Centogene AG - the Rare Disease Company in Germany.

NTHL1, POLE, POLD1, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, FLCN, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM, BLM, FH , (...)

View the complete list with 11 more genes
Specificity
17 %
Genes
46 %
Pancreatic cancer Panel.

By CeGaT GmbH in Germany.

PALLD, PRSS1, SPINK1, CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
30 %
Genes
46 %
Colon Cancer Panel.

By CeGaT GmbH in Germany.

AXIN1, RINT1, POLE, POLD1, SMAD4, BMPR1A, CHEK2, FLCN, STK11, NBN, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
27 %
Genes
46 %
Invitae Constitutional Mismatch Repair-Deficiency Panel.

By Invitae in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Invitae Sarcoma Panel.

By Invitae in United States.

DICER1, WRN, PDGFRA, KIT, NF1, PRKAR1A, SDHD, CDKN1C, SUFU, PTCH1, NBN, HRAS, BLM, SDHA, SDHB, FH, SDHC, RB1, TP53, RECQL4 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
46 %
Invitae Renal/Urinary Tract Cancers Panel.

By Invitae in United States.

DIS3L2, DICER1, BAP1, SMARCB1, SMARCA4, CDC73, GPC3, MET, FLCN, CDKN1C, TSC1, TSC2, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 4 more genes
Specificity
21 %
Genes
46 %
Invitae Prostate Cancer Panel.

By Invitae in United States.

HOXB13, CHEK2, NBN, ATM, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
42 %
Genes
46 %
Invitae Nervous System/Brain Cancer Panel.

By Invitae in United States.

DICER1, SMARCB1, SMARCA4, SMARCE1, NF1, PRKAR1A, SUFU, NF2, PHOX2B, PTCH1, ALK, TSC1, TSC2, HRAS, MEN1, RB1, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Invitae Pediatric Solid Tumors Panel.

By Invitae in United States.

DIS3L2, DICER1, WRN, AXIN2, BAP1, SMARCB1, SMARCA4, SMARCE1, NF1, CDC73, PRKAR1A, SMAD4, BMPR1A, MAX, GPC3, SDHD, CDKN1C, STK11, SUFU, NF2 , (...)

View the complete list with 28 more genes
Specificity
11 %
Genes
46 %
Invitae Colorectal Cancer Panel.

By Invitae in United States.

AXIN2, POLE, GREM1, POLD1, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
28 %
Genes
46 %
Invitae Syndromic Combined Immunodeficiency (CID) Panel.

By Invitae in United States.

DCLRE1B, SP110, ZBTB24, SPINK5, DNMT3B, PGM3, ACD, TTC7A, SMARCAL1, EPG5, WIPF1, NFKBIA, FOXN1, ORAI1, STAT5B, POLE, STIM1, NOP10, NHP2, CTC1 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
10 %
Colorectal cancer, Hereditary nonpolyposis: PMS2 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

PMS2
Specificity
100 %
Genes
10 %
Lynch Syndrome: MLH1, MSH2, MSH6, and PMS2 Full Gene Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
High Risk Colorectal Cancer: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC
Specificity
27 %
Genes
37 %
Pancreatic Cancer: Sequencing Panel and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

BAP1, PRSS1, SMAD4, CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, APC, BRCA2, BRCA1
Specificity
27 %
Genes
37 %
Kidney Renal Cancer NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

BAP1, MITF, MET, FLCN, SDHD, TSC1, TSC2, SDHA, SDHB, FH, SDHC, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, VHL
Specificity
27 %
Genes
46 %
PMS2 Full Gene Sequencing.

By Fulgent Genetics Fulgent Genetics in United States.

PMS2
Specificity
100 %
Genes
10 %
Renal/Kidney NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

BAP1, SMARCB1, MITF, CDC73, MET, FLCN, SDHD, TSC1, TSC2, SDHA, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1, MSH6, PMS2, MSH2 , (...)

View the complete list with 2 more genes
Specificity
23 %
Genes
46 %
Colorectal Cancer Focus Panel.

By Fulgent Genetics Fulgent Genetics in United States.

AXIN2, POLE, POLD1, SMAD4, BMPR1A, CHEK2, STK11, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
32 %
Genes
46 %
Prostate Cancer Focus Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CHEK2, NBN, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
50 %
Genes
46 %
Hematologic Malignancy Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TERT, TERC, NF1, CEBPA, GATA2, NBN, ATM, HRAS, BLM, TP53, RUNX1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
32 %
Genes
46 %
Gastric Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

PDGFRA, KIT, NF1, SMAD4, BMPR1A, STK11, CDH1, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
36 %
Genes
46 %
Endometrial Cancer Comprehensive Panel.

By Fulgent Genetics Fulgent Genetics in United States.

POLD1, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
50 %
Genes
46 %
LYNCH SYNDROME, PMS2 SEQUENCING AND DELETION/DUPLICATION.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

PMS2
Specificity
100 %
Genes
10 %
GIvantage Hereditary Colon Cancer Panel.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

SMAD4, BMPR1A, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
39 %
Genes
46 %
Hereditary Renal Cancer Panel.

By Blueprint Genetics in Finland.

REST, DIS3L2, DICER1, BAP1, SMARCB1, SMARCA4, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, TSC1, TSC2, SDHB, FH, SDHC, WT1, TP53, PTEN , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
46 %
Hereditary Cancer High Risk Panel.

By Blueprint Genetics in Finland.

POLE, POLD1, BAP1, RAD51D, RAD51C, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, ATM, MEN1, RET, TP53, PTEN, MUTYH, MLH1 , (...)

View the complete list with 8 more genes
Specificity
18 %
Genes
46 %
COLOTRUE™.

By Pathway Genomics in United States.

MDM2, SMAD4, BMPR1A, CHEK2, STK11, CDH1, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, EPCAM, APC
Specificity
34 %
Genes
46 %
Focus::HERSite® NGS Panel.

By Cancer Genetics, Inc. Cancer Genetics, Inc. in United States.

RAD51D, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, ATM, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, BRCA2, BRCA1
Specificity
25 %
Genes
37 %
Hereditary Non-Polyposis Colorectal Cancer (HNPCC) or Lynch Syndrome.

By GeneKor MSA in Greece.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Lynch Syndrome.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
PMS2 Mutation & Del/Dup Analysis.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Cancer.

By Color Genomics, Inc. Color Genomics, Inc. in United States.

POLE, GREM1, POLD1, BAP1, MITF, RAD51D, BARD1, RAD51C, BRIP1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN , (...)

View the complete list with 9 more genes
Specificity
18 %
Genes
46 %
Otogenetics Hereditary Cancers.

By Otogenetics in United States.

PALLD, RAD51, NF1, NTRK1, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, MET, CDKN2A, CDK4, STK11, CDH1, PALB2, PTCH1, NBN , (...)

View the complete list with 19 more genes
Specificity
13 %
Genes
46 %
Hereditary Non-Polyposis Colon Cancer, Sequencing PMS2 Gene.

By Reference Laboratory Genetics in Spain.

PMS2
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer , Deletions-Duplications (MLPA) PMS2 Gene.

By Reference Laboratory Genetics in Spain.

PMS2
Specificity
100 %
Genes
10 %
Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes.

By Reference Laboratory Genetics in Spain.

CEP57, DDB2, DIS3L2, XPC, RHBDF2, CYLD, BUB1B, XPA, ERCC5, DICER1, WRN, AIP, EXT1, EXT2, EGFR, ERCC4, BAP1, FANCD2, FANCI, FANCL , (...)

View the complete list with 70 more genes
Specificity
6 %
Genes
46 %
Hereditary Non-Polyposis Colon Cancer , Panel Massive Sequencing (NGS) MLH1, MSH2, MSH6, PMS2 Genes.

By Reference Laboratory Genetics in Spain.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Hereditary Gastric Cancer , Panel Massive Sequencing (NGS) 8 Genes.

By Reference Laboratory Genetics in Spain.

SMAD4, BMPR1A, CDH1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
63 %
Genes
46 %
Lynch syndrome/HNPCC.

By Labor Dr. Wisplinghoff in Germany.

MLH1, MSH6, PMS2, MSH2
Specificity
100 %
Genes
37 %
Phosphorus Leukemia Panel.

By Phosphorus Diagnostics LLC in United States.

TERT, TERC, DKC1, NF1, CEBPA, GATA2, NBN, ATM, TINF2, HRAS, BLM, TP53, RUNX1, MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
28 %
Genes
46 %
Phosphorus Ovarian/Uterine Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

DICER1, SMARCA4, RAD51D, RAD51C, BRIP1, PALB2, TP53, PTEN, MLH1, MSH6, PMS2, MSH2, EPCAM, BRCA2, BRCA1
Specificity
34 %
Genes
46 %
Phosphorus Brain and Nervous System Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

DICER1, AIP, CDKN1B, SMARCB1, SMARCA4, SMARCE1, NF1, PRKAR1A, MAX, SDHD, SUFU, NF2, PHOX2B, PTCH1, ALK, TSC1, TSC2, HRAS, SDHA, MEN1 , (...)

View the complete list with 15 more genes
Specificity
15 %
Genes
46 %
Phosphorus Pancreatic Cancer including Chronic Pancreatitis Genes Panel.

By Phosphorus Diagnostics LLC in United States.

CTRC, PRSS1, SPINK1, CASR, NF1, SMAD4, BMPR1A, CDKN2A, STK11, PALB2, ATM, TSC1, TSC2, CFTR, MEN1, TP53, MLH1, MSH6, PMS2, MSH2 , (...)

View the complete list with 5 more genes
Specificity
20 %
Genes
46 %
Phosphorus Pancreatic Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

NF1, SMAD4, BMPR1A, CDKN2A, STK11, PALB2, ATM, TSC1, TSC2, MEN1, TP53, MLH1, MSH6, PMS2, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
25 %
Genes
46 %
Phosphorus Renal/Urinary Tract Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

DIS3L2, DICER1, BAP1, SMARCB1, SMARCA4, MITF, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, TSC1, TSC2, SDHA, SDHB, FH, SDHC, WT1, TP53 , (...)

View the complete list with 7 more genes
Specificity
19 %
Genes
46 %
Phosphorus Pan-Cancer Panel.

By Phosphorus Diagnostics LLC in United States.

DIS3L2, HOXB13, DICER1, WRN, POT1, AIP, AXIN2, POLE, PDGFRA, EGFR, GREM1, POLD1, CDKN1B, BAP1, XRCC2, KIT, SMARCB1, SMARCA4, SMARCE1, TERT , (...)

View the complete list with 63 more genes
Specificity
7 %
Genes
46 %
Phosphorus Common/High Risk Cancers Panel.

By Phosphorus Diagnostics LLC in United States.

POLE, GREM1, POLD1, BAP1, MITF, RAD51D, BARD1, RAD51C, BRIP1, RAD50, SMAD4, BMPR1A, CHEK2, CDKN2A, CDK4, STK11, CDH1, PALB2, NBN, ATM , (...)

View the complete list with 12 more genes
Specificity
16 %
Genes
46 %
Phosphorus Pediatric Cancers Panel.

By Phosphorus Diagnostics LLC in United States.

DIS3L2, DICER1, WRN, AXIN2, BAP1, SMARCB1, TERT, TERC, EZH2, NF1, CDC73, PRKAR1A, CEBPA, GATA2, SMAD4, BMPR1A, MAX, GPC3, SDHD, CDKN1C , (...)

View the complete list with 33 more genes
Specificity
10 %
Genes
46 %
Renal Cancer: Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BUB1B, BAP1, SMARCB1, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, PALB2, TSC1, TSC2, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 3 more genes
Specificity
18 %
Genes
37 %
High Risk Colorectal Cancer: Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, PMS2, MSH2, APC
Specificity
27 %
Genes
37 %
Lynch Syndrome: MLH1, MSH2, MSH6, PMS2, and EPCAM Sequencing and Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, PMS2, MSH2, EPCAM
Specificity
100 %
Genes
46 %
Pancreatic Cancer: Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

PRSS1, CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, PMS2, MSH2, APC, VHL, BRCA2, BRCA1
Specificity
29 %
Genes
37 %
Lynch Syndrome: PMS2 Gene Sequencing.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

PMS2
Specificity
100 %
Genes
10 %
EPCAM Deletion Analysis.

By Baylor Miraca Genetics Laboratories in United States.

EPCAM
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer (Lynch syndrome).

By Center for Human Genetics, Inc in United States.

EPCAM
Specificity
100 %
Genes
10 %
Lynch syndrome.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom.

MLH1, MSH6, MSH2, EPCAM
Specificity
100 %
Genes
37 %
EPCAM deletion/duplication.

By Ambry Genetics in United States.

EPCAM
Specificity
100 %
Genes
10 %
EPCAM. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Diarrhea 5, with tufting enteropathy, congenital (sequence analysis of EPCAM gene).

By CGC Genetics in Portugal.

EPCAM
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colon cancer, type 8 (sequence analysis of EPCAM gene).

By CGC Genetics in Portugal.

EPCAM
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis: EPCAM gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Lynch Syndrome, EPCAM-Related: EPCAM Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

EPCAM
Specificity
100 %
Genes
10 %
Gastrointestinal and Colorectal Cancer: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

POLD1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
22 %
Genes
37 %
Hereditary Cancer Syndrome: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

BUB1B, POLD1, BAP1, XRCC2, SMARCB1, RAD51D, BARD1, RAD51C, CDC73, PRKAR1A, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, GPC3, MET, FLCN, SDHD , (...)

View the complete list with 35 more genes
Specificity
8 %
Genes
37 %
EPCAM.

By Fulgent Genetics Fulgent Genetics in United States.

EPCAM
Specificity
100 %
Genes
10 %
Gastrointestinal and Colorectal Cancer: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

POLD1, SMAD4, BMPR1A, CHEK2, CDKN2A, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, MSH2, EPCAM, APC, BRCA2, BRCA1
Specificity
22 %
Genes
37 %
High Risk Colorectal Cancer: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, MSH2, EPCAM, APC
Specificity
27 %
Genes
37 %
Lynch Syndrome: EPCAM Gene Deletion/Duplication.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

EPCAM
Specificity
100 %
Genes
10 %
Lynch Syndrome: MLH1, MSH2, MSH6, and EPCAM Sequencing and Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, MSH2, EPCAM
Specificity
100 %
Genes
37 %
Hereditary Cancer Syndrome: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BUB1B, POLD1, BAP1, XRCC2, SMARCB1, RAD51D, BARD1, RAD51C, CDC73, PRKAR1A, BRIP1, RAD50, SMAD4, BMPR1A, MAX, CHEK2, GPC3, MET, FLCN, SDHD , (...)

View the complete list with 35 more genes
Specificity
8 %
Genes
37 %
EPCAM deletion/duplication analysis.

By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center in United States.

EPCAM
Specificity
100 %
Genes
10 %
EPCAM.

By Institute for Human Genetics University Clinic Freiburg in Germany.

EPCAM
Specificity
100 %
Genes
10 %
Breast and Ovarian Hereditary Cancer Panel, Sequencing and Deletion/Duplication, 20 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

RAD51D, BARD1, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, NBN, ATM, MEN1, TP53, PTEN, MUTYH, MLH1, MSH6, MSH2, EPCAM, BRCA2, BRCA1
Specificity
20 %
Genes
37 %
MSH2 gene sequence and MSH2 and EPCAM deletion/duplication and MSH2 Inversion.

By Ambry Genetics in United States.

MSH2, EPCAM
Specificity
100 %
Genes
19 %
EPCAM. Deletion of the 3 region of the gene by MLPA.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Congenital Diarrhea Seq Analysis.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SPINT2, GUCY2C, DGAT1, SLC9A3, STX3, MYO5B, SLC26A3, PNLIP, SLC5A1, LCT, SAR1B, SKIV2L, TTC37, SI, NEUROG3, APOB, FLNA, MTTP, PCSK1, CFTR , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Congenital Diarrhea Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SPINT2, GUCY2C, DGAT1, SLC9A3, STX3, MYO5B, SLC26A3, PNLIP, SLC5A1, LCT, SAR1B, SKIV2L, TTC37, SI, NEUROG3, APOB, FLNA, MTTP, PCSK1, CFTR , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Congenital Diarrhea Seq + Del/Dup Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SPINT2, GUCY2C, DGAT1, SLC9A3, STX3, MYO5B, SLC26A3, PNLIP, SLC5A1, LCT, SAR1B, SKIV2L, TTC37, SI, NEUROG3, APOB, FLNA, MTTP, PCSK1, CFTR , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer (HNPCC, deletion/duplication analysis on MLH1, MSH2 and EPCAM genes).

By CGC Genetics in Portugal.

MLH1, MSH2, EPCAM
Specificity
100 %
Genes
28 %
Lynch Syndrome via EPCAM Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

EPCAM
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis type 8.

By Centogene AG - the Rare Disease Company in Germany.

EPCAM
Specificity
100 %
Genes
10 %
Cancer Predisposition.

By Asper Biogene Asper Biogene LLC in Estonia.

DDB2, DIS3L2, XPC, RHBDF2, CYLD, XPA, ERCC5, DICER1, WRN, AIP, EXT1, EXT2, EGFR, ERCC4, BAP1, FANCD2, FANCI, FANCL, FANCM, SLX4 , (...)

View the complete list with 69 more genes
Specificity
5 %
Genes
37 %
Lynch Syndrome: MLH, MSH2, MSH6, and EPCAM Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1, MSH6, MSH2, EPCAM
Specificity
100 %
Genes
37 %
Lynch Syndrome: MLH1, MSH2, MSH6, PMS2, and EPCAM Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1, MSH6, MSH2, EPCAM
Specificity
100 %
Genes
37 %
High Risk Colorectal Cancer: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SMAD4, BMPR1A, CHEK2, STK11, CDH1, ATM, BLM, TP53, PTEN, MUTYH, MLH1, MSH6, MSH2, EPCAM, APC
Specificity
27 %
Genes
37 %
Cholestasis Panel.

By Blueprint Genetics in Finland.

SPINT2, MYO5B, NR1H4, SLC26A3, LCT, CREB3L3, HSD3B7, NOTCH2, TTC37, ABCC2, BAAT, VIPAS39, VPS33B, NEUROG3, LMF1, AKR1D1, PEX5, PEX12, PEX10, PEX26 , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
10 %
Congenital Diarrhea Panel.

By Blueprint Genetics in Finland.

SLC10A2, ADAM17, IL21, SPINT2, GUCY2C, DGAT1, SLC9A3, STX3, MYO5B, SLC26A3, SLC5A1, LCT, SAR1B, IL10, IL10RB, SKIV2L, TTC7A, TTC37, SI, IL10RA , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer type VIII.

By Bioarray in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Intestinal epithelial dysplasia.

By Bioarray in Spain.

EPCAM
Specificity
100 %
Genes
10 %
EPCAM Mutation & Del/Dup Analysis.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

EPCAM
Specificity
100 %
Genes
10 %
INTESTINAL EPITHELIAL DYSPLASIA.

By Laboratorio de Genetica Clinica SL in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Congenital Intractable Familial Diarrhea with Epithelial Abnormalities, Sequencing EPCAM Gene.

By Reference Laboratory Genetics in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer, Deletion (MLPA) EPCAM Gene.

By Reference Laboratory Genetics in Spain.

EPCAM
Specificity
100 %
Genes
10 %
Familial Prostate Cancer , Panel Massive Sequencing (NGS) 11 Genes.

By Reference Laboratory Genetics in Spain.

MSR1, CHEK2, CDH1, NBN, AR, ZFHX3, RNASEL, ELAC2, EPCAM, BRCA2, BRCA1
Specificity
10 %
Genes
10 %
Pancreatic Cancer: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

PRSS1, CDKN2A, STK11, PALB2, ATM, TP53, MLH1, MSH6, MSH2, EPCAM, APC, VHL, BRCA2, BRCA1
Specificity
29 %
Genes
37 %
Karyomegalic Tubulointerstitial Nephritis (KTN) via FAN1 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

FAN1
Specificity
100 %
Genes
10 %
Nephronophthisis and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

TRAF3IP1, MAPKBP1, FAN1, ANKS6, CEP83, ZNF423, CEP164, GLIS2, CEP41, NEK8, RPGRIP1L, TMEM138, TTC21B, SDCCAG8, WDR19, DCDC2, OFD1, AHI1, TMEM216, PKHD1 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
Interstitial nephritis, karyomegalic.

By Institute of Human Genetics Cologne University in Germany.

FAN1
Specificity
100 %
Genes
10 %
Interstitial nephritis karyomegalic.

By Centogene AG - the Rare Disease Company in Germany.

FAN1
Specificity
100 %
Genes
10 %
Nephronophthisis Panel.

By CeGaT GmbH in Germany.

SLC41A1, FAN1, ANKS6, CEP83, ZNF423, CEP164, GLIS2, NEK8, TTC21B, WDR19, DCDC2, IQCB1, XPNPEP3, NPHP4, CEP290, NPHP1, NPHP3, TMEM67, INVS
Specificity
6 %
Genes
10 %
FAN1.

By Fulgent Genetics Fulgent Genetics in United States.

FAN1
Specificity
100 %
Genes
10 %
KidneySeq - 264 Genes.

By Iowa Institute of Human Genetics University of Iowa in United States.

FN1, FAN1, DSTYK, CHD1L, SIX2, ARHGAP24, NUP107, NUP93, NUP205, FAT1, XPO5, SGPL1, TRAP1, UPK3A, AGTR1, TBX18, EHHADH, ANLN, FGF20, KCTD1 , (...)

View the complete list with 232 more genes
Specificity
1 %
Genes
10 %
Nephronophthisis and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TRAF3IP1, MAPKBP1, FAN1, ANKS6, CEP83, ZNF423, CEP164, GLIS2, CEP41, NEK8, RPGRIP1L, TMEM138, TTC21B, SDCCAG8, WDR19, DCDC2, OFD1, AHI1, TMEM216, PKHD1 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
Nephronophthisis and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TRAF3IP1, MAPKBP1, FAN1, ANKS6, CEP83, ZNF423, CEP164, GLIS2, CEP41, NEK8, RPGRIP1L, TMEM138, TTC21B, SDCCAG8, WDR19, DCDC2, OFD1, AHI1, TMEM216, PKHD1 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
10 %
Nephrotic Syndrome Panel.

By Blueprint Genetics in Finland.

FN1, FAN1, ARHGAP24, NUP107, SGPL1, ANLN, PTPRO, EMP2, MAFB, ARHGDIA, MYO1E, WDR73, CRB2, SMARCAL1, ITGA3, COQ8B, TTC21B, APOL1, DGKE, CD2AP , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
10 %
MLH1 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Sequence Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Sequencing and Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Promoter Hypermethylation.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Sequencing.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Deletion/Duplication Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1/MSH2 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1, MSH2
Specificity
100 %
Genes
19 %
MLH1-Related Lynch syndrome.

By Genetics Laboratory University of Oklahoma Health Sciences Center in United States.

MLH1
Specificity
100 %
Genes
10 %
Germline mismatch repair gene mutation.

By Service de Génétique Gustave Roussy in France.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
MLH1 Related Lynch Syndrome.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

MLH1
Specificity
100 %
Genes
10 %
MutL, E. COLI, HOMOLOG OF, 1; MLH1.

By Human Genetics Ruhr University in Germany.

MLH1
Specificity
100 %
Genes
10 %
Renal Hereditary Cancer Panel, Sequencing and Deletion/Duplication, 15 Genes.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

BAP1, MET, FLCN, SDHD, TSC1, TSC2, SDHB, FH, SDHC, TP53, PTEN, MLH1, MSH6, MSH2, VHL
Specificity
20 %
Genes
28 %
HNPCC/Lynch Syndrome (MLH1) Sequencing and Deletion/Duplication.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1, MSH2, MSH6. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Hereditary Kidney Cancer Panel.

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

BAP1, SMARCB1, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, TSC1, TSC2, SDHA, SDHB, FH, SDHC, WT1, PTEN, MLH1, MSH6, MSH2, VHL
Specificity
15 %
Genes
28 %
MLH1-Related Lynch Syndrome.

By Laboratory of Genetics HUSLAB in Finland.

MLH1
Specificity
100 %
Genes
10 %
Neurofibromatosis and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

SPRED1, NF1, NF2, MLH1, MSH6, MSH2
Specificity
50 %
Genes
28 %
Neurofibromatosis and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

SPRED1, NF1, NF2, MLH1, MSH6, MSH2
Specificity
50 %
Genes
28 %
MLH1 promoter methylation.

By Molecular Diagnostics Laboratory University Health Network in Canada.

MLH1
Specificity
100 %
Genes
10 %
Hereditary non-polyposis Colon Cancer.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Prostate cancer panel.

By Centogene AG - the Rare Disease Company in Germany.

HOXB13, CHEK2, NBN, TP53, PTEN, MLH1, MSH6, MSH2, BRCA2, BRCA1
Specificity
30 %
Genes
28 %
Colorectal cancer, hereditary nonpolyposis type 2.

By Centogene AG - the Rare Disease Company in Germany.

MLH1
Specificity
100 %
Genes
10 %
MLH1.

By Innovagenomics Innovagenomics S.L in Spain.

MLH1
Specificity
100 %
Genes
10 %
Lynch dyndrome, Colorectal Cancer, MLH1.

By GGA - Galil Genetic Analysis in Israel.

MLH1
Specificity
100 %
Genes
10 %
MLH1-Related Lynch Syndrome.

By ProntoLab - MLPA Lab Pronto Diagnostics Ltd. in Israel.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Hereditary Non-Polyposis Colon Cancer (HNPCC),MLH1 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 2.

By Praxis fuer Humangenetik Wien in Austria.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis: MLH1 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome: MLH1, MSH2, and MSH6 Full Gene Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Lynch Syndrome: MLH1, MSH2, and MSH6 Gene Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Brain, CNS, and PNS Cancer: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, ATM, ALK, MEN1, TP53, MLH1, MSH6, MSH2, APC, VHL
Specificity
20 %
Genes
28 %
Lynch Syndrome, MLH1 Sequencing and Deletion/Duplication.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

MLH1
Specificity
100 %
Genes
10 %
Lynch syndrome.

By Bioarray in Spain.

MLH1
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer, Sequencing MLH1 Gene.

By Reference Laboratory Genetics in Spain.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome: MLH1, MSH2, and MSH6 Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Lynch Syndrome: MLH1, MSH2, and MSH6 Gene Sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Lynch Syndrome: MLH1 Gene Deletion/Duplication.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 full gene sequencing.

By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1, MSH2, and MSH6 Sequencing Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
MLH1 Promoter Methylation Studies.

By Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories in United States.

MLH1
Specificity
100 %
Genes
10 %
Hereditary Nonpolyposis Colorectal Cancer (HNPCC): MLH1 (Known Mutation).

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1/MSH2/MSH6 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
MLH1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

MLH1
Specificity
100 %
Genes
10 %
Microsatellite Instability (MSI) Analysis.

By Ambry Genetics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Promoter Hypermethylation.

By Ambry Genetics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 gene sequence and deletion/duplication.

By Ambry Genetics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

MLH1
Specificity
100 %
Genes
10 %
MLH1. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MLH1
Specificity
100 %
Genes
10 %
MLH1, MSH2. MLPA testing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MLH1, MSH2
Specificity
100 %
Genes
19 %
Hereditary Non-polyposis Colorectal Cancer, HNPCC (sequence analysis of MLH1 gene).

By CGC Genetics in Portugal.

MLH1
Specificity
100 %
Genes
10 %
Hereditary Non-polyposis Colorectal Cancer, HNPCC (sequence analysis of MLH1 and MSH2 genes).

By CGC Genetics in Portugal.

MLH1, MSH2
Specificity
100 %
Genes
19 %
Hereditary nonpolyposis colorectal cancer (HNPCC, NGS panel for 3 genes).

By CGC Genetics in Portugal.

MLH1, MSH6, MSH2
Specificity
100 %
Genes
28 %
Methylation analysis of the MLH1 gene promotor by ms-MLPA.

By CGC Genetics in Portugal.

MLH1
Specificity
100 %
Genes
10 %
Muir-Torre syndrome (sequence analysis of MLH1 and MSH2 genes).

By CGC Genetics in Portugal.

MLH1, MSH2
Specificity
100 %
Genes
19 %
MLH1 Related Lynch Syndrome.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, type 2.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome via MLH1 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MLH1
Specificity
100 %
Genes
10 %
Neurofibromatosis and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

SPRED1, NF1, NF2, MLH1, MSH6, MSH2
Specificity
50 %
Genes
28 %
MLH1-Related Lynch Syndrome.

By MGZ Medical Genetics Center in Germany.

MLH1
Specificity
100 %
Genes
10 %
MLH1-Related Lynch Syndrome.

By Bioscientia GmbH Center for Human Genetics in Germany.

MLH1
Specificity
100 %
Genes
10 %
Muir-Torré syndrome.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

MLH1, MSH2
Specificity
100 %
Genes
19 %
Test for MLH1-Related Lynch Syndrome.

By All Wales Genetics Laboratory Institute of Medical Genetics in United Kingdom.

MLH1
Specificity
100 %
Genes
10 %
MLH1-Related Lynch Syndrome.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

MLH1
Specificity
100 %
Genes
10 %
MLH1/MSH2 Deletion Duplication (MLPA).

By Advanced Molecular Diagnostics Mount Sinai Hospital in Canada.

MLH1
Specificity
100 %
Genes
10 %
MLH1 gene sequencing.

By Advanced Molecular Diagnostics Mount Sinai Hospital in Canada.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome.

By Department of Clinical Genetics St. Elisabeth Cancer Institute in Slovakia.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 2.

By MedGene in Slovakia.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis- MLH1 and MSH2 genes deletions-duplications analysis (MLPA).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MLH1, MSH2
Specificity
100 %
Genes
19 %
Lynch Syndrome: MLH1 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1
Specificity
100 %
Genes
10 %
Lynch Syndrome: MLH1 Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1 Full Gene Sequencing.

By Fulgent Genetics Fulgent Genetics in United States.

MLH1
Specificity
100 %
Genes
10 %
MLH1.

By Fulgent Genetics Fulgent Genetics in United States.

MLH1
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, type 2.

By Bioarray in Spain.

MLH1
Specificity
100 %
Genes
10 %
Lynch syndrome.

By Bioarray in Spain.

MLH1
Specificity
100 %
Genes
10 %
Breast Cancer Panel.

By ApolloGen, Inc. in United States.

RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, NBN, ATM, TP53, PTEN, MLH1, MSH6, MSH2, BRCA2, BRCA1
Specificity
20 %
Genes
28 %
MLH1 Mutation & Del/Dup Analysis.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

MLH1
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer, Deletions-Duplications (MLPA) MLH1 Gene.

By Reference Laboratory Genetics in Spain.

MLH1
Specificity
100 %
Genes
10 %
Renal Cancer: Gene Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

BUB1B, BAP1, SMARCB1, CDC73, GPC3, MET, FLCN, SDHD, CDKN1C, PALB2, TSC1, TSC2, SDHB, FH, SDHC, WT1, TP53, PTEN, MLH1, MSH6 , (...)

View the complete list with 2 more genes
Specificity
14 %
Genes
28 %
Brain, CNS, and PNS Cancer: Deletion/Duplication Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SUFU, PALB2, NF2, PHOX2B, PTCH1, NBN, ATM, ALK, MEN1, TP53, MLH1, MSH6, MSH2, APC, VHL
Specificity
20 %
Genes
28 %
Lynch Syndrome: MLH1 Gene Sequencing.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MLH1
Specificity
100 %
Genes
10 %
MSH6 Comprehensive - Sequence & Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Sequencing and Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Sequencing.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Comprehensive Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Deletion/Duplication Analysis.

By Molecular Diagnostic Laboratory LabCorp in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6-Related Lynch syndrome.

By Genetics Laboratory University of Oklahoma Health Sciences Center in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6-Related Lynch Syndrome.

By Molecular Genetics Rabin Medical Center in Israel.

MSH6
Specificity
100 %
Genes
10 %
MSH6.

By Institute for Human Genetics University Clinic Freiburg in Germany.

MSH6
Specificity
100 %
Genes
10 %
HNPCC/Lynch Syndrome (MSH6) Sequencing and Deletion/Duplication.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 gene sequence and deletion/duplication.

By Ambry Genetics in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

MSH6
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer (HNPCC, sequence analysis of MSH6 gene).

By CGC Genetics in Portugal.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome via MSH6 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MSH6
Specificity
100 %
Genes
10 %
Test for MSH6-Related Lynch Syndrome.

By All Wales Genetics Laboratory Institute of Medical Genetics in United Kingdom.

MSH6
Specificity
100 %
Genes
10 %
MSH6-Related Lynch Syndrome.

By ProntoLab - MLPA Lab Pronto Diagnostics Ltd. in Israel.

MSH6
Specificity
100 %
Genes
10 %
Ashkenazi Jewish diseases.

By Asper Biogene Asper Biogene LLC in Estonia.

F11, MEFV, CYP21A2, LRRK2, TOR1A, TMEM216, ABCC8, MCOLN1, SERPINA1, NEB, FKTN, SMN1, LDLR, GJB2, BLM, GBA, FANCC, CFTR, ELP1, ASPA , (...)

View the complete list with 17 more genes
Specificity
6 %
Genes
19 %
MSH6-Related Lynch Syndrome.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Gene Sequencing.

By Advanced Molecular Diagnostics Mount Sinai Hospital in Canada.

MSH6
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 5.

By Praxis fuer Humangenetik Wien in Austria.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome.

By Department of Clinical Genetics St. Elisabeth Cancer Institute in Slovakia.

MSH6
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 5.

By MedGene in Slovakia.

MSH6
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis: MSH 6 gene deletions-duplications analysis (MLPA).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome: MSH6 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome: MSH6 Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Full Gene Sequencing.

By Fulgent Genetics Fulgent Genetics in United States.

MSH6
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer type V.

By Bioarray in Spain.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Mutation & Del/Dup Analysis.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.

MSH6
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer, Deletions-Duplications (MLPA) MSH6 Gene.

By Reference Laboratory Genetics in Spain.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Sequence Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 Sequence Analysis (Familial Mutation/Variant Analysis).

By Baylor Miraca Genetics Laboratories in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 full gene sequencing.

By Clinical Molecular Diagnostic Laboratory City of Hope National Medical Center in United States.

MSH6
Specificity
100 %
Genes
10 %
Hereditary Nonpolyposis Colorectal Cancer (HNPCC): MSH6 (Known Mutation).

By Molecular Diagnostic Laboratory LabCorp in United States.

MSH6
Specificity
100 %
Genes
10 %
MSH6 - Related Lynch Syndrome.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

MSH6
Specificity
100 %
Genes
10 %
MutS, E. COLI, HOMOLOG OF, 6; MSH6.

By Human Genetics Ruhr University in Germany.

MSH6
Specificity
100 %
Genes
10 %
MSH6. MLPA testing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MSH6
Specificity
100 %
Genes
10 %
MSH6. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MSH6
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer, type 5 (HNPCC, deletion/duplication analysis on MSH6 gene).

By CGC Genetics in Portugal.

MSH6
Specificity
100 %
Genes
10 %
MSH6-Related Lynch Syndrome.

By MGZ Medical Genetics Center in Germany.

MSH6
Specificity
100 %
Genes
10 %
Breast ovarian cancer panel.

By Centogene AG - the Rare Disease Company in Germany.

RAD51, BARD1, RAD51C, BRIP1, CHEK2, STK11, CDH1, PALB2, NBN, MRE11, ATM, TP53, PTEN, MSH6
Specificity
8 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis type 5.

By Centogene AG - the Rare Disease Company in Germany.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome, Colorectal Cancer, MSH6.

By GGA - Galil Genetic Analysis in Israel.

MSH6
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis: MSH 6 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

MSH6
Specificity
100 %
Genes
10 %
MSH6.

By Fulgent Genetics Fulgent Genetics in United States.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome, MSH6 Sequencing and Deletion/Duplication.

By Quest Diagnostics Nichols Institute San Juan Capistrano in United States.

MSH6
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer, Sequencing MSH6 Gene.

By Reference Laboratory Genetics in Spain.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome: MSH6 Gene Sequencing.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MSH6
Specificity
100 %
Genes
10 %
Lynch Syndrome: MSH6 Gene Deletion/Duplication.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

MSH6
Specificity
100 %
Genes
10 %
MSH2 Deletion/Duplication Analysis.

By Baylor Miraca Genetics Laboratories in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Sequencing and Deletion/Duplication.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2 - Related Lynch Syndrome.

By Molecular Genetics Laboratory London Health Sciences Centre in Canada.

MSH2
Specificity
100 %
Genes
10 %
MutS, E. COLI, HOMOLOG OF, 2; MSH2.

By Human Genetics Ruhr University in Germany.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Exons 1-7 Inversion Analysis.

By GeneDx in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

MSH2
Specificity
100 %
Genes
10 %
MSH2-Related Lynch Syndrome.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

MSH2
Specificity
100 %
Genes
10 %
Lynch Syndrome via the MSH2 Exons 1-7 Inversion.

By PreventionGenetics PreventionGenetics in United States.

MSH2
Specificity
100 %
Genes
10 %
Lynch Syndrome via MSH2 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2-Related Lynch Syndrome.

By Bioscientia GmbH Center for Human Genetics in Germany.

MSH2
Specificity
100 %
Genes
10 %
Test for MSH2-Related Lynch Syndrome.

By All Wales Genetics Laboratory Institute of Medical Genetics in United Kingdom.

MSH2
Specificity
100 %
Genes
10 %
MSH2-Related Lynch Syndrome.

By ProntoLab - MLPA Lab Pronto Diagnostics Ltd. in Israel.

MSH2
Specificity
100 %
Genes
10 %
Hereditary Non-Polyposis Colon Cancer (HNPCC),MSH2 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

MSH2
Specificity
100 %
Genes
10 %
MSH2-Related Lynch Syndrome.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Gene Sequencing.

By Advanced Molecular Diagnostics Mount Sinai Hospital in Canada.

MSH2
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 1.

By Praxis fuer Humangenetik Wien in Austria.

MSH2
Specificity
100 %
Genes
10 %
Lynch Syndrome.

By Department of Clinical Genetics St. Elisabeth Cancer Institute in Slovakia.

MSH2
Specificity
100 %
Genes
10 %
Colorectal cancer, hereditary nonpolyposis, 1.

By MedGene in Slovakia.

MSH2
Specificity
100 %
Genes
10 %
Lynch Syndrome: MSH2 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Full Gene Sequencing.

By Fulgent Genetics Fulgent Genetics in United States.

MSH2
Specificity
100 %
Genes
10 %
MSH2.

By Fulgent Genetics Fulgent Genetics in United States.

MSH2
Specificity
100 %
Genes
10 %
Lynch syndrome type 1.

By Bioarray in Spain.

MSH2
Specificity
100 %
Genes
10 %
Hereditary nonpolyposis colorectal cancer type I.

By Bioarray in Spain.

MSH2
Specificity
100 %
Genes
10 %
MSH2 Mutation & Del/Dup Analysis.

By NeoGenomics Laboratories NeoGenomics Laboratories, Inc. in United States.