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Results: 101 to 111 of 111

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pseudohypoaldosteronism Type 2 NGS Panel

Fulgent Genetics
United States
139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cholestasis NGS Panel

Fulgent Genetics
United States
12166
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lung Disorders NGS Panel

Fulgent Genetics
United States
7651
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bronchiectasis NGS Panel

Fulgent Genetics
United States
2016
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliopathies NGS Panel

Fulgent Genetics
United States
14197
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bronchiectasis with or without elevated sweat chloride 1

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

CFTR-Related Hereditary Pancreatitis

MGZ Medical Genetics Center
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CFTR-Related Disorders

MGZ Medical Genetics Center
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Bronchiectasis

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
13
  • C Sequence analysis of the entire coding region

Results: 101 to 111 of 111

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.