Clinical and research tests for C0023976 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
LQTS panel Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS Italy	1	13	D Deletion/duplication analysis C Sequence analysis of the entire coding region
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
Comprehensive Cardiomyopathy Panel Mayo Clinic Laboratories Mayo Clinic United States	68	83	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
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
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
Brugada Syndrome, SCN5A Full Gene Mayo Clinic Laboratories Mayo Clinic United States	12	1	D Deletion/duplication analysis 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
PGmax™ - Comprehensive Congenital Heart Disease Panel PreventionGenetics, part of Exact Sciences United States	24	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
CPVT Panel - Catecholaminergic Plymorphic Ventricular Tachycardia Panel GeneDx United States	5	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Rest of Arrhythmia after CPVT Panel GeneDx United States	5	48	D Deletion/duplication analysis 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
Rest of Arrhythmia Panel after LQTS Panel GeneDx United States	5	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Rest of Combined Cardiac after Arrhythmia Panel GeneDx United States	5	80	D Deletion/duplication analysis 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
Rest of Arrhythmia after Brugada Syndrome Panel GeneDx United States	5	41	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

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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.