Clinical and research tests for C2675520 - 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
3 Ashkenazi BRCA1 and BRCA2 mutations Genetic Services Laboratory University of Chicago United States	2	2	T Targeted variant analysis
Hereditary Breast and Ovarian Cancer BRCA1&2 GeneKor MSA Greece	5	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Common Hereditary Cancer Screening Panel PreventionGenetics, part of Exact Sciences United States	94	55	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Congenital Anomalies of the Gastrointestinal Tract Panel PreventionGenetics, part of Exact Sciences United States	297	180	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Inherited Bone Marrow Failure Panel PreventionGenetics, part of Exact Sciences United States	267	186	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Medulloblastoma Panel PreventionGenetics, part of Exact Sciences United States	21	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Wilms Tumor Panel PreventionGenetics, part of Exact Sciences United States	48	28	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
BRCA Portuguese 1-mutation panel specific site analysis Ambry Genetics United States	8	1	T Targeted variant analysis
BRCA Ashkenazi Jewish 3-mutation panel Ambry Genetics United States	11	2	T Targeted variant analysis
Prostate Cancer Panel PreventionGenetics, part of Exact Sciences United States	20	16	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Breast Cancer - High / Moderate Risk Panel PreventionGenetics, part of Exact Sciences United States	13	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Breast and Ovarian Cancer - Expanded and Lynch Syndrome Panel PreventionGenetics, part of Exact Sciences United States	29	33	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Breast and Ovarian Cancer - High Risk and Lynch Syndrome Panel PreventionGenetics, part of Exact Sciences United States	19	17	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Melanoma Panel PreventionGenetics, part of Exact Sciences United States	11	10	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Endometrial Cancer Panel PreventionGenetics, part of Exact Sciences United States	17	12	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Ovarian Cancer Panel PreventionGenetics, part of Exact Sciences United States	40	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hereditary Breast and Ovarian Cancer BRCA1/2 Panel PreventionGenetics, part of Exact Sciences United States	4	2	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Pancreatic Cancer Panel PreventionGenetics, part of Exact Sciences United States	27	18	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cancer Panel PreventionGenetics, part of Exact Sciences United States	122	117	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis

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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.