Clinical and research tests for 808 - 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
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
Catecholaminergic polymorphic ventricular tachycardia panel Health in Code Spain	1	9	C Sequence analysis of the entire coding region
Arrhythmia General Panel Health in Code Spain	1	218	C Sequence analysis of the entire coding region
Cardiovascular Diseases_General Panel Health in Code Spain	1	380	C Sequence analysis of the entire coding region
Ventricular arrhythmia and sudden death without structural heart disease Health in Code Spain	1	77	C Sequence analysis of the entire coding region
Long QT Syndrome Extended Panel Health in Code Spain	1	28	C Sequence analysis of the entire coding region
Catecholaminergic Polymoprhic Ventricular Tachycardia Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	3	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
GenepoweRx_Cardiac Care GenepoweRx Uppaluri K&H Personalized Medicine Clinic India	63	102	D Deletion/duplication analysis H Detection of homozygosity S Mutation scanning of the entire coding region T Targeted variant analysis
CALM3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CentoCardio Panel Centogene AG - the Rare Disease Company Germany	289	275	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	4	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome Panel PreventionGenetics, part of Exact Sciences United States	22	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia via the CALM3 Gene PreventionGenetics, part of Exact Sciences United States	1	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiac channelopathy Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Catecholaminergic polymorphic ventricular tachycardia Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	1	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiac channelopathy NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	41	C Sequence analysis of the entire coding region T Targeted variant analysis
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

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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.