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Results: 161 to 180 of 180

Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51284672
  • 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

Myofibrillar myopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
177
  • C Sequence analysis of the entire coding region

Neuromuscular NGS Panel

Fulgent Genetics
United States
259112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Mucopolysaccharidosis NGS Panel

Fulgent Genetics
United States
2114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital heart defects panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
6934
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Cardiomyopathy panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
12861
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Atrial Fibrillation NGS Panel

Fulgent Genetics
United States
8424
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myofibrillar Panel

FirmaLab
United States
16
  • C Sequence analysis of the entire coding region

Distal Myopathy Panel

FirmaLab
United States
1111
  • 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

Hypertrophic Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
13098
  • C Sequence analysis of the entire coding region

Dilated Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
10073
  • C Sequence analysis of the entire coding region

Left Ventricular Noncompaction Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
5136
  • C Sequence analysis of the entire coding region

Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
551
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LDB3-Related Dilated Cardiomyopathy

FirmaLab
United States
21
  • C Sequence analysis of the entire coding region

Arrhythmogenic Right Ventricular Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3218
  • C Sequence analysis of the entire coding region

LDB3-Related Dilated Cardiomyopathy

John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
United States
11
  • C Sequence analysis of the entire coding region

Zaspopathy

John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine
United States
11
  • C Sequence analysis of the entire coding region

Results: 161 to 180 of 180

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.