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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Cardiomyopathy NGS Panel

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

Long QT/Brugada Syndrome NGS Panel

Fulgent Genetics
United States
6934
  • 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

RNF125 Single Gene

Fulgent Genetics
United States
291
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GPD1L Single Gene

Fulgent Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • 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

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

Results: 1 to 9 of 9

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.