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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

Female Infertility Panel

CGC Genetics Unilabs
Portugal
1129
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Female Infertility panel

Genetic Services Laboratory University of Chicago
United States
1093
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Premature Ovarian Failure Panel

GeneDx
United States
622
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Premature ovarian failure: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1715
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Premature Ovarian Failure: Sequencing Panel and FMR1 CGG Repeat Analysis

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
121
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

GDF9 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Premature Ovarian Failure Panel

Genetic Services Laboratory University of Chicago
United States
1026
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

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.