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Results: 21 to 40 of 99

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hereditary Breast and Ovarian Cancer - Expanded and Lynch Syndrome Panel

PreventionGenetics, part of Exact Sciences
United States
2933
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Myeloid Malignancy Panel

Genetic Services Laboratory University of Chicago
United States
3785
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Ovarian Cancer Panel

PreventionGenetics, part of Exact Sciences
United States
4030
  • 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

Male Infertility Panel

PreventionGenetics, part of Exact Sciences
United States
128139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cancer Panel

PreventionGenetics, part of Exact Sciences
United States
122117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fanconi Anemia via the FANCM Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Breast Cancer - Expanded Risk Panel

PreventionGenetics, part of Exact Sciences
United States
1621
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fanconi Anemia Panel

PreventionGenetics, part of Exact Sciences
United States
2022
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fanconi anemia (NGS panel for 22 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
122
  • C Sequence analysis of the entire coding region

Oncological diseases panel _v.2.0

CGC Genetics Unilabs
Portugal
1205
  • C Sequence analysis of the entire coding region

Male Infertility Panel

CGC Genetics Unilabs
Portugal
1165
  • C Sequence analysis of the entire coding region

Gynecological (Breast, Ovarian, Endometrial) Cancer Panel 

CGC Genetics Unilabs
Portugal
136
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Syndrome Panel 

CGC Genetics Unilabs
Portugal
1175
  • C Sequence analysis of the entire coding region

Anemia Panel

CGC Genetics Unilabs
Portugal
1174
  • C Sequence analysis of the entire coding region

Spermatogenic failure 28 , Premature ovarian failure (deletion/duplication analysis of FANCM gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

Fanconi anemia type M (sequence analysis of FANCM gene)

CGC Genetics Unilabs
Portugal
11
  • 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

Endocrine Neoplasia Panel (Expanded)

Mendelics
Brazil
158
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 99

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.