Clinical and research tests for C0003811 - 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
Arrhythmogenic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	26	18	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
Comprehensive Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	68	83	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CPVT Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	11	7	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
Dilated Cardiomyopathy/LVNC Panel Mayo Clinic Laboratories Mayo Clinic United States	52	63	D Deletion/duplication analysis C Sequence analysis of the entire coding region
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
Brugada Syndrome, SCN5A Full Gene Mayo Clinic Laboratories Mayo Clinic United States	12	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CustomNext-Cardio® Ambry Genetics United States	236	167	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndromes panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	16	C Sequence analysis of the entire coding region
Catecholaminergic Polymorphic Ventricular Tachycardia panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	7	C Sequence analysis of the entire coding region
Brugada Syndromes panel Clinical Genomics Laboratory Washington University in St. Louis United States	2	17	C Sequence analysis of the entire coding region
Cardiac Diseases Gene panel Clinical Genomics Laboratory Washington University in St. Louis United States	12	150	C Sequence analysis of the entire coding region
TruGenome Cardiovascular Disease Test Illumina Laboratory Services Illumina United States	4	1	C Sequence analysis of the entire coding region
Arrhythmia Panel Mendelics Brazil	1	311	C Sequence analysis of the entire coding region
Inherited Cadiac Disorders Panel Dhiti Omics Technologies Private Ltd India	60	33	C Sequence analysis of the entire coding region
Comprehensive Metabolism NGS Panel Fulgent Genetics United States	602	355	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Early-Onset Ataxia NGS Panel Fulgent Genetics United States	505	132	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Schwannomatosis NGS Panel Fulgent Genetics United States	85	7	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.