Clinical and research tests for C0949658 - 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
Hypertrophic Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	44	48	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
CentoCardio Panel Centogene AG - the Rare Disease Company Germany	289	275	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Hereditary Heart Health Test Color Diagnostics, LLC DBA Color Health United States	19	30	C Sequence analysis of the entire coding region
Targeted Cardiomyopathy panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	4	41	S Mutation scanning of the entire coding region
Cardiomyopathy Exome Panel Northwest Clinical Genomics Laboratory University of Washington United States	31	75	C Sequence analysis of the entire coding region
Invitae Hypertrophic Cardiomyopathy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	75	59	D Deletion/duplication analysis C Sequence analysis of the entire coding region
SCO2 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	2	1	S Mutation scanning of the entire coding region
MYL3 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	1	1	S Mutation scanning of the entire coding region
MYH7 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	1	S Mutation scanning of the entire coding region
MYBPC3 Sequencing Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	1	S Mutation scanning of the entire coding region
Comprehensive Cardiomyopathy Panel (37 genes) Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	4	37	X Mutation scanning of select exons S Mutation scanning of the entire coding region
Hereditary Disease Risk Test Color Diagnostics, LLC DBA Color Health United States	51	59	C Sequence analysis of the entire coding region
Hypertrophic Cardiomyopathy Panel, Sequencing ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	25	34	C Sequence analysis of the entire coding region
mtDNA Targeted Analysis: Known Familial Mutation Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	11	34	T Targeted variant analysis
mtDNA Targeted Analysis with Heteroplasmy: Known Familial Mutation Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	11	34	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.