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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypomagnesemia NGS Panel

Fulgent Genetics
United States
12123
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Short Rib Dysplasia / Asphyxiating Thoracic Dysplasia NGS Panel

Fulgent Genetics
United States
18815
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis NGS Panel

Fulgent Genetics
United States
33961
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WDR60 Single Gene

Fulgent Genetics
United States
561
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WDR34 Single Gene

Fulgent Genetics
United States
571
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNH1 Single Gene

Fulgent Genetics
United States
751
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IFT172 Single Gene

Fulgent Genetics
United States
851
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ATP6V1B2 Single Gene

Fulgent Genetics
United States
511
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

P4HB Single Gene

Fulgent Genetics
United States
341
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAM111A Single Gene

Fulgent Genetics
United States
901
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CEP120 Single Gene

Fulgent Genetics
United States
431
  • 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

Retinitis Pigmentosa NGS Panel

Fulgent Genetics
United States
329124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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.