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Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

Rhizomelic chondrodysplasia punctata type 2 (RCDP2, sequence analysis of GNPAT gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

RINT1 Gene Breast cancer, RINT1 related NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Tempus xT

Tempus AI - CHI
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Invitae Hyperammonemia Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
7572
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone diseases panel_v.2.0

CGC Genetics Unilabs
Portugal
1662
  • C Sequence analysis of the entire coding region

Hereditary cancer panel

CIBIC S.A.
Argentina
178
  • C Sequence analysis of the entire coding region

Heriditary cancer extended panel

CIBIC S.A.
Argentina
1111
  • C Sequence analysis of the entire coding region

RINT1 Single Gene

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

Breast and Ovarian Cancer - extended Diagnostic Panel

CeGaT GmbH
Germany
741
  • C Sequence analysis of the entire coding region

Colorectal Cancer

CeGaT GmbH
Germany
1119
  • C Sequence analysis of the entire coding region

Results: 1 to 11 of 11

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.