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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

NGS Panel for Fanconi anemia

BloodGenetics
Spain
2222
  • C Sequence analysis of the entire coding region

NGS Panel for Bone Marrow failure

BloodGenetics
Spain
5769
  • C Sequence analysis of the entire coding region

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

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

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

Bone Marrow Failure NGS Panel

Fulgent Genetics
United States
18060
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia

Asper Biogene Asper Biogene LLC
Estonia
1717
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi anemia Panel

CeGaT GmbH
Germany
1716
  • C Sequence analysis of the entire coding region

FANCM Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

Cancer Predisposition

Asper Biogene Asper Biogene LLC
Estonia
13598
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FANCM Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fanconi Anemia Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
1615
  • S Mutation scanning of the entire coding region

Fanconi Anemia NGS Panel

Fulgent Genetics
United States
3018
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 17 of 17

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.