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Results: 1 to 20 of 32

Tests names and labsConditionsGenes and analytesMethods

Immunodeficiency type 3, with hyper-IgM

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

New Born testing (CentoICU)

Centogene AG - the Rare Disease Company
Germany
767514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

Tempus xO assay

Tempus Labs, Inc.
United States
11714
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Tempus xT assay

Tempus Labs, Inc.
United States
2594
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • C Sequence analysis of the entire coding region

Primary Antibody Deficiency Sequencing Panel with CNV Detection

PreventionGenetics
United States
5045
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Immune Report Card

OmniSeq, Inc.
United States
147
  • I Microsatellite instability testing (MSI)
  • R RNA analysis
  • E Sequence analysis of select exons

Hyper IgM Syndrome Sequencing Panel with CNV Detection

PreventionGenetics
United States
1111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hyper IgM Syndrome (HIGM): Three-gene Profile (AICDA, UNG, CD40) (Full Gene Sequencing)

Molecular Diagnostic Laboratory LabCorp
United States
13
  • C Sequence analysis of the entire coding region

Hyper IgM Syndrome (HIGM): Four-gene Profile (AICDA, UNG, CD40, CD40LG) (Full Gene Sequencing)

Molecular Diagnostic Laboratory LabCorp
United States
14
  • C Sequence analysis of the entire coding region

Hyper IgM Syndrome (HIGM): (CD40 [TNFRSF5] for HIGM3) (Known mutation)

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

Hyper IgM Syndrome (HIGM): (CD40 [TNFRSF5] for HIGM3) (Full Gene Sequencing)

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

Primary Antibody Deficiency NGS Panel

Fulgent Genetics
United States
10237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1050472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Severe Combined Immunodeficiency NGS Panel

Fulgent Genetics
United States
33090
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyper IgM Syndrome ,Panel Massive Sequencing (NGS) 4 Genes

Reference Laboratory Genetics
Spain
44
  • C Sequence analysis of the entire coding region

Common Variable Immune Deficiency and Related Disorders, Panel Massive Sequencing (NGS) 41 Genes

Reference Laboratory Genetics
Spain
4341
  • C Sequence analysis of the entire coding region

Immunodeficiency with hyper-IgM, type 3 (sequence analysis of CD40 gene)

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

Immunodeficiency with hyper-IgM, type 3 (sequence analysis of CD40 gene)

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

HYPER-IgM SYNDROME TYPE 3 (AUTOSOMAL RECESSIVE)

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

Results: 1 to 20 of 32

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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