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Results: 1 to 20 of 58 (representing 21 labs)

Tests names and labsConditionsGenes and analytesMethods

Fanconi anemia type N

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast ovarian cancer panel

Centogene AG - the Rare Disease Company
Germany
1914
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1918
  • C Sequence analysis of the entire coding region

Cancer Sequencing and Deletion/Duplication Panel

PreventionGenetics
United States
4335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fanconi Anemia via the PALB2/FANCN Gene

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

Fanconi Anemia Sequencing Panel

PreventionGenetics
United States
1719
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Chromosomes, DEB Assay for Fanconi Anemia

Quest Diagnostics Nichols Institute Chantilly
United States
1515
  • B Chromosome breakage studies

Chromosome DEB Assay for Fanconi anemia, Prenatal

Quest Diagnostics Nichols Institute Chantilly
United States
1515
  • B Chromosome breakage studies

Certain forms of hereditary breast cancer and pancreatic cancer - PALB2 gene

Hereditary Cancer Group - Genetic Diagnostic Unit Germans Trias I Pujol Research Institute
Spain
21
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Fanconi Anemia

Asper Biotech Asper Biotech Ltd.
Estonia
1717
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Breast/Ovarian Cancer Panel

Genetic Services Laboratory University of Chicago
United States
1618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCA1, BRCA2, and PALB2 Mutation Analysis

Genetic Services Laboratory University of Chicago
United States
63
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Breast and Ovarian Cancer High Risk Panel

Genetic Services Laboratory University of Chicago
United States
97
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Myelodysplastic Syndrome/Leukemia Panel

Invitae
United States
2621
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Bone Marrow Failure Syndromes Panel

Invitae
United States
4939
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia Comprehensive Panel

Fulgent Genetics
United States
20017
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast Cancer Comprehensive Panel

Fulgent Genetics
United States
51618
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cancer Panel

Fulgent Genetics
United States
1736124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatic Cancer Comprehensive Panel

Fulgent Genetics
United States
61422
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

COLON, BREAST AND OVARIAN CANCER

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
3531
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 58

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.

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