Clinical and research tests for C0022387 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Comprehensive Arrhythmia Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	36	44	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiomyopathy and Arrhythmia Panel Mayo Clinic Laboratories Mayo Clinic United States	73	105	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	12	10	D Deletion/duplication analysis E Sequence analysis of select exons
Short QT Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	8	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome and Jervell and Lange-Nielsen syndrome via the KCNQ1 Gene PreventionGenetics, part of Exact Sciences United States	4	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
OtoGenome Test for Hearing Loss (110 Genes) Laboratory for Molecular Medicine Mass General Brigham Personalized Medicine United States	23	109	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Jervell and Lange-Nielsen Syndrome (KCNQ1) Targeted Testing DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States	1	1	T Targeted variant analysis
Hearing Loss Test GeneDx United States	56	150	D Deletion/duplication analysis E Sequence analysis of select exons C Sequence analysis of the entire coding region
Syndromic Hearing Loss NGS Panel Fulgent Genetics United States	223	83	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Hearing Loss NGS Panel Fulgent Genetics United States	332	167	D Deletion/duplication analysis C Sequence analysis of the entire coding region
ACMG Secondary Findings (Medically Actionable Genes, Including Cardio and Cancer) NGS Panel Fulgent Genetics United States	177	59	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States	450	128	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT/Brugada Syndrome NGS Panel Fulgent Genetics United States	69	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel Fulgent Genetics United States	118	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Jervell and Lange-Nielsen Syndrome: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	2	C Sequence analysis of the entire coding region
LONG QT SYNDROME, JERVELL AND LANGE-NIELSEN SYNDROME (AUTOSOMAL RECESSIVE) Laboratorio de Genetica Clinica SL Spain	1	2	C Sequence analysis of the entire coding region
Long QT Syndrome 1 (KCNQ1) Targeted Testing DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States	2	1	T Targeted variant analysis
Cardiomyopathy and Arrhythmia Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	125	83	D Deletion/duplication analysis C Sequence analysis of the entire coding region
KCNQ1 Single Gene Fulgent Genetics United States	5	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Jervell and Lange-Nielsen Syndrome NGS Panel Fulgent Genetics United States	7	2	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.