Clinical and research tests for C1512419 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Hereditary Cancer Panel Comprehensive Molecular Genetics Laboratory London Health Sciences Centre Canada	39	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Prostate Cancer panel Genetic Services Laboratory University of Chicago United States	1	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PREVENTEST GeneID Lab - Advanced Molecular Diagnostics United States	60	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Melanoma Panel Genetic Services Laboratory University of Chicago United States	9	16	D Deletion/duplication analysis C Sequence analysis of the entire coding region
myRisk Hereditary Cancer Myriad Genetics, Inc. United States	32	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Solid Tumor Panel Centogene AG - the Rare Disease Company Germany	218	135	C Sequence analysis of the entire coding region
ColoGene GeneID Lab - Advanced Molecular Diagnostics United States	41	19	C Sequence analysis of the entire coding region
Melanoma Cancer Panel IntelligeneCG LLC United States	13	9	C Sequence analysis of the entire coding region
Hereditary melanoma (5 gènes) Center for Human Genetics Cliniques Universitaires Saint Luc Belgium	1	5	C Sequence analysis of the entire coding region
myRisk Single Site Analysis Myriad Genetics, Inc. United States	32	45	T Targeted variant analysis
Guideline Based Hereditary Cancer Panel (32 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States	20	32	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Hereditary Cancer Panel (66 Genes) Quest Diagnostics Nichols Institute San Juan Capistrano United States	35	66	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CDKN2A Sequencing and Deletion/Duplication Quest Diagnostics Nichols Institute San Juan Capistrano United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Phosphorus Melanoma Panel Phosphorus Diagnostics LLC United States	1	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
TSPAN31 Single Gene Fulgent Genetics United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Melanoma Panel Invitae United States	15	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Multi-Cancer Panel Invitae United States	139	80	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Common Hereditary Cancers Panel (Breast, Gyn, GI) Invitae United States	75	42	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Melanoma-Pancreatic Cancer Syndrome Panel Invitae United States	4	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Dyskeratosis Congenita panel by next-generation sequencing (NGS) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	15	15	C Sequence analysis of the entire coding region

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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.