Clinical and research tests for C2348199 - 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
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
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
CPVT Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	11	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Long QT Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	12	10	D Deletion/duplication analysis E Sequence analysis of select exons
Short QT Syndrome Gene Panel Mayo Clinic Laboratories Mayo Clinic United States	8	4	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Short QT syndome Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	1	5	C Sequence analysis of the entire coding region
Long QT Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	4	11	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Cardiac channelopathies panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	9	33	S Mutation scanning of the entire coding region
Short QT syndrome NGS panel HNL Genomics Connective Tissue Gene Tests United States	13	6	C Sequence analysis of the entire coding region T Targeted variant analysis
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
Cardiac Diseases Gene panel Clinical Genomics Laboratory Washington University in St. Louis United States	12	150	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
SCA Arrhythmia Panel GeneDx United States	5	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmia Sequencing and Del/Dup Panel GeneDx United States	5	58	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Combined Cardiac Sequencing and Del/Dup Panel GeneDx United States	10	138	D Deletion/duplication analysis C Sequence analysis of the entire coding region
KCNH2 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
KCNQ1 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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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.