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Results: 81 to 88 of 88

Tests names and labsConditionsGenes, analytes, and microbesMethods

SNTA1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
747
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Sudden Death Syndrome NGS Panel

Fulgent Genetics
United States
16868
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cardiac conduction abnormalities panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
7633
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
671250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Arrhythmia NGS Panel

Fulgent Genetics
United States
18476
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
2519
  • C Sequence analysis of the entire coding region

Results: 81 to 88 of 88

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.