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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.
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9 labs with tests matching your search, 2 labs matching in other ways
Lab name Tests matching your search
CGC Genetics Portugal1
CeGaT GmbH Germany2
DNA Labs India India1
Fulgent Genetics United States7
Institute for Human Genetics Germany1
Intergen Genetics and Rare Diseases Diagnosis Center Turkey2
Labcorp Genetics (formerly Invitae) United States7
Otogenetics Corporation United States1
PreventionGenetics, part of Exact Sciences United States2
Breda Genetics srl Italy0
Victorian Clinical Genetics Services Australia0
Results:
24 genetic tests from 9 labs with tests matching your search, 2 labs matching in other ways
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Compare between 2 to 5 tests using the icon in the search results to make your selection.
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Download data for all or selected tests, using the check boxes in the search results to make your selection.
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51274672
  • D Deletion/duplication analysis
  • 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

Invitae Primary Immunodeficiency Panel

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

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

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

Invitae Ectodermal Dysplasia and Related Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
14873
  • D Deletion/duplication analysis

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics Corporation
United States
123129
  • E Sequence analysis of select exons

Combined Immunodeficiencies with Syndromic Features Panel

PreventionGenetics, part of Exact Sciences
United States
11070
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Inherited Ichthyoses and Related Disorders Panel

PreventionGenetics, part of Exact Sciences
United States
12668
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Phagocytic Disorders Including Neutropenia Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
9268
  • 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

Syndromes with immunodeficiency Panel

CeGaT GmbH
Germany
3338
  • C Sequence analysis of the entire coding region

Netherton syndrome, 256500, Autosomal recessive; NETH (Netherton syndrome) (SPINK5 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Netherton syndrome, 256500, Autosomal recessive; NETH (Netherton syndrome) (SPINK5 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Invitae Congenital Ichthyosis Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
7745
  • D Deletion/duplication analysis

Ichthyosis NGS Panel

Fulgent Genetics
United States
9843
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hyper IgE Syndrome Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
1611
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ichthyoses and related disorders of cornification Panel

CeGaT GmbH
Germany
4265
  • C Sequence analysis of the entire coding region

SPINK5 Gene Netherton syndrome NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Hyper-IgE Syndrome NGS Panel

Fulgent Genetics
United States
305
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
24 tests from 9 labs
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❮Page 1 of 2❯
Clinical Exome by Fulgent Genetics
5127 conditions, 4672 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
Invitae Primary Immunodeficiency Panel by Labcorp Genetics (formerly Invitae), LabCorp
552 conditions, 424 genes
Comprehensive Primary Immunodeficiency NGS Panel by Fulgent Genetics
1048 conditions, 472 genes
Invitae Comprehensive Severe Combined Immunodeficiency (SCID) and Combined Immunodeficiency (CID) Panel by Labcorp Genetics (formerly Invitae), LabCorp
177 conditions, 130 genes
Invitae Ectodermal Dysplasia and Related Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
148 conditions, 73 genes
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel by Otogenetics Corporation
123 conditions, 129 genes
Combined Immunodeficiencies with Syndromic Features Panel by PreventionGenetics, part of Exact Sciences
110 conditions, 70 genes
Inherited Ichthyoses and Related Disorders Panel by PreventionGenetics, part of Exact Sciences
126 conditions, 68 genes
Invitae Phagocytic Disorders Including Neutropenia Panel by Labcorp Genetics (formerly Invitae), LabCorp
92 conditions, 68 genes
Severe Combined Immunodeficiency NGS Panel by Fulgent Genetics
330 conditions, 90 genes
Syndromes with immunodeficiency Panel by CeGaT GmbH
33 conditions, 38 genes
Netherton syndrome, 256500, Autosomal recessive; NETH (Netherton syndrome) (SPINK5 gene) (Sequence Analysis-All Coding Exons) (Prenatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Netherton syndrome, 256500, Autosomal recessive; NETH (Netherton syndrome) (SPINK5 gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Invitae Congenital Ichthyosis Panel by Labcorp Genetics (formerly Invitae), LabCorp
77 conditions, 45 genes
Ichthyosis NGS Panel by Fulgent Genetics
98 conditions, 43 genes
Invitae Hyper IgE Syndrome Panel by Labcorp Genetics (formerly Invitae), LabCorp
16 conditions, 11 genes
Ichthyoses and related disorders of cornification Panel by CeGaT GmbH
42 conditions, 65 genes
SPINK5 Gene Netherton syndrome NGS Genetic DNA Test by DNA Labs India
1 condition, 1 gene
Hyper-IgE Syndrome NGS Panel by Fulgent Genetics
30 conditions, 5 genes

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.