Clinical and research tests for C1959582 - 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
PREVENTEST GeneID Lab - Advanced Molecular Diagnostics United States	60	34	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
PTEN gene sequence and deletion/duplication Ambry Genetics United States	11	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VistaSeq GYN Panel Molecular Diagnostic Laboratory LabCorp United States	11	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VistaSeq Breast Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	16	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VisaSeq Breast and GYN Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	32	25	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PTEN Sequencing and Deletion/Duplication on Blood Medical Genomics Laboratory Department of Genetics UAB United States	5	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Vistaseq Hereditary Cancer Panel Without BRCA Molecular Diagnostic Laboratory LabCorp United States	17	25	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VistaSeq Hereditary Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	18	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Gastric Cancer Panel Genetic Services Laboratory University of Chicago United States	10	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Vascular Malformations Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	24	28	D Deletion/duplication analysis C Sequence analysis of the entire coding region
PTEN Hamartoma Tumur Syndrome (PHTS) Genetic Pathology SA Pathology Australia	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Thyroid Cancer Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	7	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Melanoma Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	11	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Central Nervous System Cancer Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	23	27	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Breast Cancer High-Risk Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	4	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Breast Cancer Guidelines-Based Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	7	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Breast Cancer Management Panel GeneDx United States	24	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
VistaSeq Endrocrine Cancer Panel Molecular Diagnostic Laboratory LabCorp United States	12	13	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.