Clinical and research tests for C1832916 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Short QT syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States	13	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Short QT syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	13	6	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hypertrophic Cardiomyopathy Panel PreventionGenetics, part of Exact Sciences United States	66	60	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
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
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
Invitae Cardiomyopathy Comprehensive Panel Invitae United States	198	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Invitae United States	239	100	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Arrhythmia Comprehensive Panel Invitae United States	115	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Short QT Syndrome Panel PreventionGenetics, part of Exact Sciences United States	5	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Comprehensive Cardiac Arrhythmia Panel PreventionGenetics, part of Exact Sciences United States	77	64	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Timothy Syndrome and Brugada Syndrome via the CACNA1C Gene PreventionGenetics, part of Exact Sciences United States	2	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Hypertrophic Cardiomyopathy Panel Invitae United States	69	30	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Inherited Cadiac Disorders Panel Dhiti Omics Technologies Private Ltd India	60	33	C Sequence analysis of the entire coding region
Arrhythmia panel. NGS panel of 55 genes. Genologica Medica Spain	128	55	C Sequence analysis of the entire coding region
Long QT syndrome panel. 16-gene NGS panel. Genologica Medica Spain	36	16	C Sequence analysis of the entire coding region
Autism Spectrum Disorders Panel. NGS panel of 26 genes. Genologica Medica Spain	39	26	C Sequence analysis of the entire coding region
Short QT syndrome panel Genologica Medica Spain	12	5	C Sequence analysis of the entire coding region
Brugada syndrome panel. 9-gene NGS panel. Genologica Medica Spain	26	9	C Sequence analysis of the entire coding region
Brugada Syndrome Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	25	14	C Sequence analysis of the entire coding region
Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	211	93	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 76

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.