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Results: 1 to 20 of 33 (representing 21 labs)

Tests names and labsConditionsGenes and analytesMethods

FoundationOne®

Foundation Medicine, Inc.
United States
1315
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
124129
  • E Sequence analysis of select exons

FoundationOne® Heme

Foundation Medicine, Inc.
United States
2405
  • D Deletion/duplication analysis
  • R RNA analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Autoimmune lymphoproliferative syndrome

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

Tier 2: Hereditary Lymphoma and Immunodeficiency Panel

Genetic Services Laboratory University of Chicago
United States
1723
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autoimmune Lymphoproliferative Syndrome via the FAS Gene

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

FAS. Complete sequencing

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

LYMPHOPROLIFERATIVE SYNDROME, AUTOIMMUNE

Laboratorio de Genetica Clinica SL
Spain
45
  • C Sequence analysis of the entire coding region

Autoimmune lymphoproliferative syndrome (deletion/duplication analysis of FAS gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Autoimmune lymphoproliferative syndrome (deletion/duplication analysis of FAS gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Autoimmune Lymphoproliferative Syndrome Type IA, Sequencing FAS Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Invitae Autoimmune Lymphoproliferative Disorders (ALPS) Panel

Invitae
United States
148
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Primary Immunodeficiency Panel

Invitae
United States
282207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Monogenic Autoimmunity Panel

Invitae
United States
10973
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Immune Dysregulation Disorders Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
3223
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Immunodeficiency Panel

Blueprint Genetics
Finland
2232
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone Marrow Failure Syndrome Panel

Blueprint Genetics
Finland
193
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hematology Panel

Blueprint Genetics
Finland
4175
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hemophagocytic Lymphohistiocytosis Panel

Blueprint Genetics
Finland
413
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autoimmune lymphoproliferative syndrome (ALPS); FAS Sequencing

Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences
Iran
11
  • S Mutation scanning of the entire coding region

Results: 1 to 20 of 33

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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