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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

Bone Marrow Failure / Anemia Panel

Centogene AG - the Rare Disease Company
Germany
212212
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MarrowZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital
United States
250155
  • C Sequence analysis of the entire coding region

Dyserythropoietic anemia, congenital, type Ib, 615631, Autosomal recessive; CDAN1B (Congenital dyserythropoietic anemia type I) (C15orf41 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Dyserythropoietic anemia, congenital, type Ib, 615631, Autosomal recessive; CDAN1B (Congenital dyserythropoietic anemia type I) (C15orf41 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hereditary Hemolytic Anemia Panel

PreventionGenetics, part of Exact Sciences
United States
4434
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

WES iron disorders

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
2046
  • E Sequence analysis of select exons

panel congenital dyserythropoietic anemia (CDAN1, C15orf41, GATA1, SEC23B, KIF23, KLF1)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
56
  • C Sequence analysis of the entire coding region

C15ORF41 - congenital dyserythropoietic anemia, type Ib

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Congenital Dyserythropoietic Anemia Type I via the CDIN1/C15orf41 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

Congenital Dyserythropoietic Anemia Panel

PreventionGenetics, part of Exact Sciences
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Dyserythropoietic anemia, congenital type Ib (sequence analysis of C15orf41 gene)

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

Inherited Red Blood Cell Disorder Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
1752
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Anemia, congenital dyserythropoietic: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Porphyria Disorders NGS Panel

Fulgent Genetics
United States
1511
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CONGENITAL DYSERYTHROPOIETIC ANEMIA, TYPE 1

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

C15orf41 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

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.