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Results: 1 to 20 of 31

Tests names and labsConditionsGenes, analytes, and microbesMethods

Infertility Panel

Centogene AG - the Rare Disease Company
Germany
243238
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

AR - Repeat expansion analysis

Centogene AG - the Rare Disease Company
Germany
51
  • T Targeted variant analysis

AR - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Disorders of Sex Development Panel

Invitae
United States
8853
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypospadias 1, X-linked, 300633, X-linked recessive; HYSP1 (Familial hypospadias) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Hypospadias 1, X-linked, 300633, X-linked recessive; HYSP1 (Familial hypospadias) (AR gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypospadias 1, X-linked, 300633, X-linked recessive; HYSP1 (Familial hypospadias) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Hypospadias 1, X-linked, 300633, X-linked recessive; HYSP1 (Familial hypospadias) (AR gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Carrier Screen

Invitae
United States
886547
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypospadias Panel

PreventionGenetics, Part of Exact Sciences
United States
15673
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ambiguous Genitalia Panel

PreventionGenetics, Part of Exact Sciences
United States
12885
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Kennedy Disease Repeat Expansion Analysis

Baylor Genetics
United States
51
  • T Targeted variant analysis

AR Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
51
  • T Targeted variant analysis

AR Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
51
  • T Targeted variant analysis

AR Sequence Analysis

Baylor Genetics
United States
51
  • C Sequence analysis of the entire coding region

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
240171
  • D Deletion/duplication analysis

Infertility

Genologica Medica
Spain
2511
  • C Sequence analysis of the entire coding region

Genital Abnormalities / Sex Development Disorders Panel

Genologica Medica
Spain
9549
  • C Sequence analysis of the entire coding region

AR deletion/duplication analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
51
  • D Deletion/duplication analysis

AR (ANDROGEN RECEPTOR) ANALYSİS

Duzen Laboratories Duzen BBAGUAS
Turkey
51
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 31

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.