Filters

See more specimen types...

Other countries

Results: 1 to 20 of 20 (representing 14 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Immunodeficiency type 2, with hyper-IgM

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

Hyper IgM Syndrome (HIGM): (AICDA for HIGM2) (Known Mutation)

Molecular Diagnostic Laboratory LabCorp
United States
11
  • E Sequence analysis of select exons

Hyper IgM Syndrome (HIGM): (AICDA for HIGM2) (Full Gene Sequencing)

Molecular Diagnostic Laboratory LabCorp
United States
11
  • C Sequence analysis of the entire coding region

Hyper IgM Syndrome via the AICDA Gene

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

AICDA. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Humoral dysfunction Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
2624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Humoral dysfunction Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
2624
  • C Sequence analysis of the entire coding region

Humoral dysfunction Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
2624
  • D Deletion/duplication analysis

Immunodeficiency with hyper-IgM, type 2

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Immunodeficiency with hyper-IgM type 2 (sequence analysis of AICDA gene)

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

Immunodeficiency with hyper IgM type 2

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Primary Antibody Deficiency Panel, Sequencing (35 Genes) and Deletion/Duplication (26 Genes)

ARUP Laboratories, Molecular Genetics and Genomics
United States
3735
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

AICDA

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

Inflammatory Bowel Disease: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
4926
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

B cell pathology panel

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
1614
  • C Sequence analysis of the entire coding region

AICDA

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
11
  • C Sequence analysis of the entire coding region

AID gene

Immunology Diagnostics Laboratory Seattle Children's Research Institute
United States
11
  • C Sequence analysis of the entire coding region

CD40 Ligand gene

Immunology Diagnostics Laboratory Seattle Children's Research Institute
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.

Support Center