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Results: 1 to 20 of 37

Tests names and labsConditionsGenes, analytes, and microbesMethods

FSHR Gene Ovarian dysgenesis type 1 NGS Genetic DNA Test

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

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

FSHR - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ovarian response to FSH stimulation, 276400, Autosomal recessive (FSHR 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

Ovarian hyperstimulation syndrome, 608115, Autosomal dominant; OHSS (Ovarian hyperstimulation syndrome) (FSHR 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

Ovarian dysgenesis 1, 233300, Autosomal recessive; ODG1 (46,XX gonadal dysgenesis) (46,XX gonadal dysgenesis) (FSHR 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

Female infertility genetic testing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
16
  • K Karyotyping
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Male infertility genetic testing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
15
  • K Karyotyping
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Premature Ovarian Failure (POF) Panel

PreventionGenetics, part of Exact Sciences
United States
1921
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Differences of Sex Development (DSD) Panel

PreventionGenetics, part of Exact Sciences
United States
149158
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Differences of Sex Development (DSD) and Infertility Panel

PreventionGenetics, part of Exact Sciences
United States
223238
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Female Infertility Panel

PreventionGenetics, part of Exact Sciences
United States
96105
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ovarian Dysgenesis and Ovarian Hyperstimulation Syndrome via the FSHR Gene

PreventionGenetics, part of Exact Sciences
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Premature ovarian failure (WES based NGS panel of 47 genes, including analysis of CNVs)

CGC Genetics Unilabs
Portugal
147
  • C Sequence analysis of the entire coding region

Female Infertility Panel

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

46,XX gonadal dysgenesis (sequence analysis of FSHR gene)

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

Ovarian dysgenesis 1 Ovarian hyperstimulation syndrome (deletion/duplication analysis on FSHR gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

HEREDITARY ATAXIAS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
11202
  • E Sequence analysis of select exons

Infertility

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

Panel of premature ovarian failure. NGS panel of 15 genes.

Genologica Medica
Spain
5015
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 37

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.