Clinical and research tests for C0041341 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
OnkoRisk Hereditary Oncology Plus Panel BioReference Health United States	97	77	C Sequence analysis of the entire coding region
OnkoRisk Hereditary Oncology Guideline Panel BioReference Health United States	71	54	C Sequence analysis of the entire coding region
Hereditary Cancer Screening - Common Hereditary Cancer Panel (41 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	47	41	X Mutation scanning of select exons
Hereditary Cancer Screening - Nervous System & Endocrine Cancer Panel (44 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	52	44	X Mutation scanning of select exons
Hereditary Cancer Screening - Renal/Urinary Tract Cancer Panel (Including prostate and kidney cancer) - (39 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	40	39	X Mutation scanning of select exons
Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	109	99	X Mutation scanning of select exons
Cystic Kidney Disease Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	16	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Tuberous Sclerosis Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	3	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region
TUBEROUS SCLEROSIS Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol Spain	3	2	D Deletion/duplication analysis E Sequence analysis of select exons 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
Known Mutation Testing- NGS Medical Genomics Laboratory Department of Genetics UAB United States	9	1	E Sequence analysis of select exons
Genetic Test of single known genetic variant National Taiwan University Hospital A1 Center National Taiwan University Hospital Taiwan	7	10	E Sequence analysis of select exons
Tuberous Sclerosis Complex(TSC) panel National Taiwan University Hospital A1 Center National Taiwan University Hospital Taiwan	3	2	C Sequence analysis of the entire coding region
Cortical Malformations and Epilepsy Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	35	39	C Sequence analysis of the entire coding region
Tuberous Sclerosis Panel Mendelics Brazil	1	2	C Sequence analysis of the entire coding region
myRisk Single Site Analysis Myriad Genetics, Inc. United States	32	45	T Targeted variant analysis
Hereditary Cystic and Glomerular Disorders Panel Genetic Services Laboratory University of Chicago United States	17	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Tuberous sclerosis Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey	1	1	C Sequence analysis of the entire coding region
Tuberous sclerosis Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center Turkey	1	1	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

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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.