Clinical and research tests for C3280785 - Genetic Testing Registry (GTR) - NCBI

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Results: 21 to 40 of 51

Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States	239	100	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Invitae Arrhythmia Comprehensive Panel Labcorp Genetics (formerly Invitae) LabCorp United States	115	41	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Isolated Nonsyndromic Congenital Heart Defects via the NKX2-5 Gene PreventionGenetics, part of Exact Sciences United States	6	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes. Genologica Medica Spain	42	21	C Sequence analysis of the entire coding region
Congenital structural heart disease panel. NGS panel of 62 genes. Genologica Medica Spain	113	62	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
Arrhythmia & Cardiomyopathy Panel, Comprehensive CNH Molecular Diagnostics Laboratory Childrens National Hospital United States	211	93	C Sequence analysis of the entire coding region
NKX2-5 Institute for Human Genetics University Medical Center Freiburg Germany	6	1	C Sequence analysis of the entire coding region
Ventricular septal defect: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	3	3	C Sequence analysis of the entire coding region
Structural Heart Disease NGS Panel Fulgent Genetics United States	73	28	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Comprehensive Primary Immunodeficiency NGS Panel Fulgent Genetics United States	1048	472	D Deletion/duplication analysis 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
Hypothyroidism and Resistance to Thyroid Hormone NGS Panel Fulgent Genetics United States	41	19	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Congenital Heart Defect NGS Panel Fulgent Genetics United States	377	114	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel Fulgent Genetics United States	118	46	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Arrhythmia Asper Biogene Asper Biogene LLC Estonia	66	38	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 Congenital Heart Defects and Heterotaxy Panel Labcorp Genetics (formerly Invitae) LabCorp United States	128	82	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Single gene testing NKX2-5 CeGaT GmbH Germany	6	1	C Sequence analysis of the entire coding region
Congenital Heart Defects Panel CeGaT GmbH Germany	42	44	C Sequence analysis of the entire coding region

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Results: 21 to 40 of 51

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.