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Results: 1 to 14 of 14

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

Facial Dysostosis and Related Disorders NGS Panel

Fulgent Genetics
United States
8529
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Oxidative Phosphorylation Disorders NGS Panel

Fulgent Genetics
United States
416235
  • 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

TCF12 Single Gene

Fulgent Genetics
United States
261
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC7A14 Single Gene

Fulgent Genetics
United States
271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ZIC1 Single Gene

Fulgent Genetics
United States
331
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IMPG1 Single Gene

Fulgent Genetics
United States
131
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IBA57 Single Gene

Fulgent Genetics
United States
221
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RHO

Fulgent Genetics
United States
331
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • 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 14 of 14

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.