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Results: 1 to 20 of 70 (representing 24 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: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
1717
  • C Sequence analysis of the entire coding region

Fanconi anemia (deletion/duplicaction analysis of FANCD2 and PALB2 genes)

CGC Genetics
Portugal
22
  • D Deletion/duplication analysis

Fanconi anemia (deletion/duplicaction analysis of FANCD2 and PALB2 genes)

CGC Genetics
Portugal
22
  • D Deletion/duplication analysis

FANCONI ANEMIA (COMPLEMENTATION GROUP N)

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Fanconi Anemia, Sequencing PALB2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Hereditary Colorectal/Gastrointestinal Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
5922
  • E Sequence analysis of select exons

Comprehensive Hereditary Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
13561
  • E Sequence analysis of select exons

Hereditary Leukemia/Lymphoma Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
3613
  • E Sequence analysis of select exons

Hereditary Pancreatic Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
4617
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Hereditary High Risk Breast Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
357
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Brain, CNS, PNS Cancer Panel

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
4317
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 70

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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