U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

Results: 21 to 40 of 56

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

Hereditary Bone Marrow Failure Panel, Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
5075
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Limb malformation panel. NGS panel of 45 genes.

Genologica Medica
Spain
7745
  • C Sequence analysis of the entire coding region

Bone marrow failure syndrome panel. NGS panel of 122 genes.

Genologica Medica
Spain
194122
  • C Sequence analysis of the entire coding region

Fanconi anemia panel

Genologica Medica
Spain
3522
  • C Sequence analysis of the entire coding region

Thrombocytopenia and inherited bone marrow failure (WES based NGS panel of 109 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
177109
  • C Sequence analysis of the entire coding region

Limb reduction defects (WES based NGS panel of 141 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
295141
  • C Sequence analysis of the entire coding region

Breast and ovary cancer (NGS panel for 27 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
6427
  • C Sequence analysis of the entire coding region

OncoRisk Expanded (NGS panel for 89 genes, including CNV analysis)

Unilabs Genetics CGC Genetics
Portugal
18289
  • C Sequence analysis of the entire coding region

Fanconi anemia type P (sequence analysis of SLX4 gene)

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

Aplastic Anemia Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
6439
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
9562
  • C Sequence analysis of the entire coding region

SLX4

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

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: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2121
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Related Disorders , Panel Massive Sequencing (NGS) 59 Genes

Reference Laboratory Genetics
Spain
6358
  • C Sequence analysis of the entire coding region

Oncology Genetic Panel , Panel Massive Sequencing (NGS) 90 Genes

Reference Laboratory Genetics
Spain
12690
  • C Sequence analysis of the entire coding region

Fanconi Anemia , Panel Massive Sequencing (NGS) 15 Genes

Reference Laboratory Genetics
Spain
1515
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 56

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.