Clinical and research tests for C5574922 - 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
Catecholaminergic polymorphic ventricular tachycardia panel Health in Code Spain	1	9	C Sequence analysis of the entire coding region
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
Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Catecholaminergic polymorphic ventricular tachycardia NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	9	C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiac channelopathies panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	9	32	S Mutation scanning of the entire coding region
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
Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States	1	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Catecholaminergic polymorphic ventricular tachycardia NGS panel HNL Genomics Connective Tissue Gene Tests United States	1	9	C Sequence analysis of the entire coding region T Targeted variant analysis
Cardiomyopathy Exome Panel Northwest Clinical Genomics Laboratory University Of Washington United States	32	75	C Sequence analysis of the entire coding region
Catecholaminergic Polymorphic Ventricular Tachycardia Panel PreventionGenetics, part of Exact Sciences United States	8	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Catecholaminergic Polymorphic Ventricular Tachycardia via the RYR2 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
Hereditary Disease Risk Test Color Diagnostics, LLC DBA Color Health United States	51	59	C Sequence analysis of the entire coding region
Targeted Variant Analysis Integrated Genetics Westborough LabCorp United States	330	746	T Targeted variant analysis
GeneSeq PLUS Integrated Genetics Westborough LabCorp United States	330	746	C Sequence analysis of the entire coding region
Partner Reflex to GeneSeq Integrated Genetics Westborough LabCorp United States	330	746	C Sequence analysis of the entire coding region
GeneSeq: Cardio - Familial Arrhythmia Panel Integrated Genetics Westborough LabCorp United States	9	51	C Sequence analysis of the entire coding region
Rest of Combined Cardiac after ARVC Panel GeneDx United States	5	121	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Rest of Arrhythmia after SCA Panel GeneDx United States	5	44	D Deletion/duplication analysis 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.