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Results: 1 to 17 of 17

Tests names and labsConditionsGenes, analytes, and microbesMethods

Lymphoma, MALT, somatic, 137245 (MALT lymphoma) (BCL10 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

Invitae Inborn Errors of Immunity and Cytopenias Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
754562
  • D Deletion/duplication analysis

Congenital Diarrhea and Enteropathies Panel

PreventionGenetics, part of Exact Sciences
United States
241157
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Comprehensive Severe Combined Immunodeficiency (SCID) and Combined Immunodeficiency (CID) Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
177130
  • D Deletion/duplication analysis

Invitae Primary Immunodeficiency Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
552424
  • D Deletion/duplication analysis

Detection by FISH of t(11;18) API2/MALT1

CGC Genetics Unilabs
Portugal
21
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of t(14;18) IGH/MALT1

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

Detection by FISH of MALT1 (18q21) rearrangements

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

IGH/MALT1 fussion

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • I FISH-interphase

Oncology FISH Analysis - MALT1 Lymphoma

Baylor Genetics
United States
11
  • T Targeted variant analysis

B-Cell Clonality Screening (IgH and IgK) by PCR

Baylor Genetics
United States
11
  • T Targeted variant analysis

Severe-Chronic EBV (CAEBV) Immunodeficiency Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
7044
  • C Sequence analysis of the entire coding region

Severe Combined Immunodeficiency (SCID) Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
3824
  • 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

BCL10 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Chromosome Analysis: Cancer

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
251
  • K Karyotyping

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.