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Results: 1 to 12 of 12

Tests names and labsConditionsGenes, analytes, and microbesMethods

CPVT Panel - Catecholaminergic Plymorphic Ventricular Tachycardia Panel

GeneDx
United States
59
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Arrhythmia after CPVT Panel

GeneDx
United States
548
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Combined Cardiac after ARVC Panel

GeneDx
United States
5121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Arrhythmia after SCA Panel

GeneDx
United States
544
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Arrhythmia Panel after LQTS Panel

GeneDx
United States
541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Combined Cardiac after Arrhythmia Panel

GeneDx
United States
580
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCA Arrhythmia Panel

GeneDx
United States
514
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rest of Arrhythmia after Brugada Syndrome Panel

GeneDx
United States
541
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Arrhythmia Sequencing and Del/Dup Panel

GeneDx
United States
558
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Long QT Syndrome (LQTS) Sequencing and Del/Dup Panel

GeneDx
United States
117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Combined Cardiac Sequencing and Del/Dup Panel

GeneDx
United States
10138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Custom Cardiology Sequencing and Del/Dup Panel

GeneDx
United States
30270
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 12 of 12

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.