Clinical and research tests for C3809536 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 53

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
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
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
Catecholaminergic polymorphic ventricular tachycardia panel. 9-gene NGS panel. Genologica Medica Spain	12	9	C Sequence analysis of the entire coding region
Cardiac arrhythmia syndrome, with or without skeletal muscle weakness: Full gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	1	1	C Sequence analysis of the entire coding region
TRDN Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States	1	1	D Deletion/duplication analysis
Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	211	93	C Sequence analysis of the entire coding region
Arrhythmia Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	71	36	C Sequence analysis of the entire coding region
Catecholaminergic polymorphic ventricular tachycardia (CPVT) Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	9	5	C Sequence analysis of the entire coding region
TRDN Institute for Human Genetics University Medical Center Freiburg Germany	1	1	C Sequence analysis of the entire coding region
Ventricular tachycardia, catecholaminergic polymorphic: Full gene sequencing panelc CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	5	5	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
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes Reference Laboratory Genetics Spain	119	95	C Sequence analysis of the entire coding region
Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes Reference Laboratory Genetics Spain	81	48	C Sequence analysis of the entire coding region
Dilated & Arrhythmogenic Cardiomyopathy NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	92	51	C Sequence analysis of the entire coding region
Catecholaminergic Polymorphic Ventricular Tachycardia Asper Biogene Asper Biogene LLC Estonia	10	6	C Sequence analysis of the entire coding region
Long QT Syndrome NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	37	18	C Sequence analysis of the entire coding region
Comprehensive Cardiac NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	174	108	C Sequence analysis of the entire coding region
Invitae Catecholaminergic Polymorphic Ventricular Tachycardia Panel Invitae United States	7	7	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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Results: 21 to 40 of 53

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.