Clinical and research tests for 125972 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	88	134	X Mutation scanning of select exons
Cardiology Sequencing- Full Panel (174 Genes) Genesys Diagnostics Genesys Diagnostics, Inc. United States	122	174	X Mutation scanning of select exons
CALR3 Gene Cardiomyopathy, familial hypertrophic type 19 NGS Genetic DNA Test DNA Labs India India	1	1	S Mutation scanning 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
Pan Cardiomyopathy Panel PreventionGenetics, part of Exact Sciences United States	113	106	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Comprehensive Cardiology Panel PreventionGenetics, part of Exact Sciences United States	223	198	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hypertrophic Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	1	42	C Sequence analysis of the entire coding region
Cardiomyopathy panel Clinical Genomics Laboratory Washington University in St. Louis United States	5	96	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
GeneSeq® Cardio Single Gene Analysis Integrated Genetics Westborough LabCorp United States	55	177	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy (WES based NGS panel of 68 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	68	C Sequence analysis of the entire coding region
Sudden death (WES based NGS panel of 80 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	80	C Sequence analysis of the entire coding region
Cardiovascular Comprehensive Panel CGC Genetics Unilabs Portugal	1	353	C Sequence analysis of the entire coding region
Cardiomyopathies Panel CGC Genetics Unilabs Portugal	1	197	C Sequence analysis of the entire coding region
Cardiomyopathy, familial hypertrophic (CMH19, sequence analysis of CALR3 gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Targeted Variant Analysis Integrated Genetics Westborough LabCorp United States	330	746	T Targeted variant analysis
Targeted Variant, Fetal Analysis Integrated Genetics Westborough LabCorp United States	292	746	T Targeted variant analysis
Partner Reflex to GeneSeq Integrated Genetics Westborough LabCorp United States	330	746	C Sequence analysis of the entire coding region
GeneSeq® Cardio: Familial Cardiomyopathy Panel Integrated Genetics Westborough LabCorp United States	17	67	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmia Panel Mendelics Brazil	1	311	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.