Clinical and research tests for C0949658 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 101

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
Common 29 mtDNA Variant Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	9	32	T Targeted variant analysis
Expanded 93 mtDNA Variant Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	11	34	T Targeted variant analysis
Congenital muscular dystrophy Asper Biogene Asper Biogene LLC Estonia	59	28	C Sequence analysis of the entire coding region
Comprehensive Cardiomyopathy NGS Panel Fulgent Genetics United States	450	128	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT/Brugada Syndrome NGS Panel Fulgent Genetics United States	69	34	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel Fulgent Genetics United States	118	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
CAV3 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	2	1	D Deletion/duplication analysis
Dilated Cardiomyopathy Asper Biogene Asper Biogene LLC Estonia	67	42	C Sequence analysis of the entire coding region
Hypertrophic cardiomyopathy - different panels Institute of Human Genetics Cologne University Germany	1	70	C Sequence analysis of the entire coding region
TNNC1 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
ANKRD1 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
PRKAG2 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
TNNI3 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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Results: 21 to 40 of 101

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.