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Results: 21 to 40 of 55

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

Invitae
United States
239100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Arrhythmia Comprehensive Panel

Invitae
United States
11541
  • 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
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atrial septal defect 7, with or without AV conduction defects (sequence analysis of NKX2-5 gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes.

Genologica Medica
Spain
4221
  • C Sequence analysis of the entire coding region

Congenital structural heart disease panel. NGS panel of 62 genes.

Genologica Medica
Spain
11362
  • C Sequence analysis of the entire coding region

Arrhythmia panel. NGS panel of 55 genes.

Genologica Medica
Spain
12855
  • C Sequence analysis of the entire coding region

Arrhythmia & Cardiomyopathy Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
21193
  • C Sequence analysis of the entire coding region

Arrhythmia Panel, Comprehensive

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
7136
  • C Sequence analysis of the entire coding region

NKX2-5

Institute for Human Genetics University Medical Center Freiburg
Germany
61
  • C Sequence analysis of the entire coding region

Atrial septal defect: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
88
  • C Sequence analysis of the entire coding region

Structural Heart Disease NGS Panel

Fulgent Genetics
United States
7328
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypothyroidism and Resistance to Thyroid Hormone NGS Panel

Fulgent Genetics
United States
4119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
377114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel

Fulgent Genetics
United States
11846
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac Conduction System Related Disorders , Panel Massive Sequencing (NGS) 20 Genes

Reference Laboratory Genetics
Spain
2620
  • C Sequence analysis of the entire coding region

Arrhythmia

Asper Biogene Asper Biogene LLC
Estonia
6638
  • C Sequence analysis of the entire coding region

Comprehensive Cardiac NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
174108
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 55

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.