Clinical and research tests for 54894 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 47

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Colorectal Cancer Panel CGC Genetics Unilabs Portugal	1	29	C Sequence analysis of the entire coding region
Hyperplastic polyposis syndrome (sequencing analysis of RNF43 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Hereditary Cancer Panel (Complete) Mendelics Brazil	1	264	C Sequence analysis of the entire coding region
Hereditary Colorectal Cancer Panel Mendelics Brazil	1	42	C Sequence analysis of the entire coding region
OnkoSight Advanced Comprehensive Solid Tumor Panel (DNA/RNA) BioReference Health United States	1	523	C Sequence analysis of the entire coding region
OnkoSight Advanced 523 Gene NGS Panel BioReference Health United States	1	523	C Sequence analysis of the entire coding region
MI Tumor Seek Hybrid Caris Life Sciences United States	1	591	R RNA analysis C Sequence analysis of the entire coding region
OncoAlly™ Solid Tumor Analysis Variantyx, Inc. United States	1	433	D Deletion/duplication analysis X Mutation scanning of select exons R RNA analysis
Hereditary Cancer Testing - Full Panel (76) AIP, APC, ATM, AXIN2, BAP1, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDC73, CDH1, CDK4, CDKN1B, CDKN2A, CHEK2, CTNN1, DICER1, EGFR, EGLN1, EPCAM, EXT1, EXT2, FH, FLCN, GALNT12, GREM1, HOXB13, KIT, LZTR1, MAX, MEN1, M Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	78	S Mutation scanning of the entire coding region
Sessile Serrated Polyposis Cancer Syndrome Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	1	S Mutation scanning of the entire coding region
Hereditary Gastrointestinal Cancer (Lynch Syndrome, Gastric, Pancreas, Polyposis, 31) APC, ATM, BMPR1A, BRCA1, BRCA2, CDH1, CDKN2A, CHEK2, CTNNA1, EPCAM, GALNT12, GREM1, MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RNF43, RP Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	31	S Mutation scanning of the entire coding region
Hereditary Breast/Ovarian/Prostate/Gastrointestinal Cancer (36) APC, ATM, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDKN2A, CHEK2, CTNNA1, EPCAM, GALNT12, GREM1, MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, NTHL1, PALB2, PMS2, POLD1, POLE, PTEN, RAD51C, RAD51D, R Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	36	S Mutation scanning of the entire coding region
Hereditary Polyposis (21) APC, BMPR1A, EPCAM, GALNT12, GREM1, MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, NTHL1, PMS2, POLD1, POLE, PTEN, RNF43, RPS20, SMAD4, STK11, TP53 Diagnostic Medical Genetics Mount Sinai Hospital, Sinai Health System Canada	1	21	S Mutation scanning of the entire coding region
Solid Tumor Expanded Panel Quest Diagnostics Nichols Institute San Juan Capistrano United States	1	523	I Microsatellite instability testing (MSI) R RNA analysis C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
NeoTYPE® Gastric Tumor Profile NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States	1	33	F Fluorescence in situ hybridization (FISH) C Sequence analysis of the entire coding region
NeoTYPE® Pancreas Tumor Profile NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States	1	63	F Fluorescence in situ hybridization (FISH) E Sequence analysis of select exons
NeoTYPE® Colorectal Tumor Profile NeoGenomics Laboratories NeoGenomics Laboratories, Inc. United States	1	36	F Fluorescence in situ hybridization (FISH) E Sequence analysis of select exons
Paired Tumor/Normal - Solid Tumor Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	2	239	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Paired Tumor/Normal - Comprehensive Solid Tumor Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States	2	315	D Deletion/duplication analysis R RNA analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 47

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