Clinical and research tests for C1141890 - 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
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
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
Long QT syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States	26	19	C Sequence analysis of the entire coding region T Targeted variant analysis
Long QT syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	26	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Long QT syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	26	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Sudden Cardiac Arrest Panel PreventionGenetics, part of Exact Sciences United States	63	49	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiac Arrhythmia Exome Panel Northwest Clinical Genomics Laboratory University Of Washington United States	39	51	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
Hereditary Disease Risk Test Color Diagnostics, LLC DBA Color Health United States	51	59	C Sequence analysis of the entire coding region
Arrhythmia Asper Biogene Asper Biogene LLC Estonia	66	38	C Sequence analysis of the entire coding region
Phosphorus Long QT Syndrome Panel Phosphorus Diagnostics LLC United States	1	15	D Deletion/duplication analysis C Sequence analysis of the entire coding region
SCN4B Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	1	1	C Sequence analysis of the entire coding region T Targeted variant analysis
CALM2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
KCNH2 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	C Sequence analysis of the entire coding region T Targeted variant analysis
KCNQ1 Gene, entire coding region or targeted variant Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute Canada	2	1	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.