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Results: 1 to 20 of 23

Tests names and labsConditionsGenes, analytes, and microbesMethods

Riboflavin Transporter Deficiency Neuronopathy NGS Panel

Fulgent Genetics
United States
482
  • 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

Retinopathy and Optic Atrophy NGS Panel

Fulgent Genetics
United States
563241
  • 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

Paroxysmal Extreme Pain Disorder NGS Panel

Fulgent Genetics
United States
18553
  • 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

SLC52A2 Single Gene

Fulgent Genetics
United States
461
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPRY4 Single Gene

Fulgent Genetics
United States
381
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TTLL5 Single Gene

Fulgent Genetics
United States
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

POC1B Single Gene

Fulgent Genetics
United States
101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HS6ST1 Single Gene

Fulgent Genetics
United States
411
  • 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

IL17RD Single Gene

Fulgent Genetics
United States
441
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PCYT1A Single Gene

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

DRAM2 Single Gene

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

DUSP6 Single Gene

Fulgent Genetics
United States
401
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGF17 Single Gene

Fulgent Genetics
United States
401
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FEZF1 Single Gene

Fulgent Genetics
United States
411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FLRT3 Single Gene

Fulgent Genetics
United States
391
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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.