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Results: 1 to 20 of 33

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

Early-Onset Ataxia NGS Panel

Fulgent Genetics
United States
507135
  • 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

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048473
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiomyopathy NGS Panel

Fulgent Genetics
United States
450128
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan and RASopathies NGS Panel

Fulgent Genetics
United States
23526
  • 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

Ataxia NGS Panel

Fulgent Genetics
United States
535152
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Heart Defect NGS Panel

Fulgent Genetics
United States
379115
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel

Fulgent Genetics
United States
24478
  • 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

RARB Single Gene

Fulgent Genetics
United States
321
  • 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

SPRY4 Single Gene

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

TCTN3 Single Gene

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

UBE2T Single Gene

Fulgent Genetics
United States
801
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HIRA Single Gene

Fulgent Genetics
United States
852
  • 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

IL17RD Single Gene

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

ARVCF Single Gene

Fulgent Genetics
United States
852
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 33

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.