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Results: 1 to 20 of 27

Tests names and labsConditionsGenes, analytes, and microbesMethods

Comprehensive Glomerular Proteinuria NGS Panel

Fulgent Genetics
United States
18276
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Syndromic Hearing Loss NGS Panel

Fulgent Genetics
United States
22383
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss NGS Panel

Fulgent Genetics
United States
332167
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Micromelic Dysplasia NGS Panel

Fulgent Genetics
United States
14024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
505132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Robinow Syndrome NGS Panel

Fulgent Genetics
United States
765
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Carpenter Syndrome NGS Panel

Fulgent Genetics
United States
452
  • 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

Ataxia NGS Panel

Fulgent Genetics
United States
533149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Coffin-Siris Syndrome NGS Panel

Fulgent Genetics
United States
8211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PTRH2 Single Gene

Fulgent Genetics
United States
241
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SOX11 Single Gene

Fulgent Genetics
United States
691
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ZBTB20 Single Gene

Fulgent Genetics
United States
641
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WDR73 Single Gene

Fulgent Genetics
United States
661
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HOXB1 Single Gene

Fulgent Genetics
United States
91
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LINS1 Single Gene

Fulgent Genetics
United States
91
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MEGF8 Single Gene

Fulgent Genetics
United States
451
  • 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

PDGFRB Single Gene

Fulgent Genetics
United States
811
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DVL1 Single Gene

Fulgent Genetics
United States
701
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 27

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.