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Results:
50 genetic tests from 25 labs with tests matching your search, 3 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Familial cold autoinflammatory syndrome 2, 611762, Autosomal dominant; FCAS2 (NLRP12-associated hereditary periodic fever syndrome) (NLRP12 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

NLRP12

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

NLRP12 Gene Cold autoinflammatory syndrome type 2 NGS Genetic DNA Test

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

NLRP12 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

NLRP12 Single Gene

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

Sanger sequencing of NLRP12

Laboratorio de Genetica Clinica SL
Spain
11
  • E Sequence analysis of select exons

Familial cold autoinflammatory syndrome 2 (sequence analysis of NLRP12 gene)

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

Somatic Inborn Errors of Immunity (IEI) Genetic Panel

Machaon Diagnostics
United States
6565
  • C Sequence analysis of the entire coding region

Autoinflammatory Gene Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
182117
  • C Sequence analysis of the entire coding region

Inborn Errors of Immunity GenePanel

Mayo Clinic Laboratories, Mayo Clinic
United States
374386
  • C Sequence analysis of the entire coding region

Multigene panel for autoinflammatory syndromes based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1101
  • S Mutation scanning of the entire coding region

Multigene panel for primary immunodeficiencies based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1535
  • S Mutation scanning of the entire coding region

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • 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 Autoinflammatory and Autoimmunity Syndromes Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
223154
  • D Deletion/duplication analysis

Invitae Primary Immunodeficiency Panel

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

Invitae Periodic Fever Syndromes Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
3218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Neuropathies (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1869
  • C Sequence analysis of the entire coding region

Haematological diseases panel

CGC Genetics, Unilabs
Portugal
1344
  • C Sequence analysis of the entire coding region

Primary immunodeficiency panel , inflammatory bowel disease , autoinflammatory disorders

CGC Genetics, Unilabs
Portugal
1491
  • C Sequence analysis of the entire coding region
50 tests from 25 labs
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NLRP12 by Genome Diagnostics Laboratory, University Medical Center Utrecht
1 condition, 1 gene
NLRP12 Sequencing by Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory, Cincinnati Children's Hospital Medical Center
1 condition, 1 gene
Sanger sequencing of NLRP12 by Laboratorio de Genetica Clinica SL
1 condition, 1 gene
Autoinflammatory Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
182 conditions, 117 genes
Inborn Errors of Immunity GenePanel by Mayo Clinic Laboratories, Mayo Clinic
374 conditions, 386 genes
Multigene panel for autoinflammatory syndromes based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 101 genes
Multigene panel for primary immunodeficiencies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 535 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
Invitae Primary Immunodeficiency Panel by Labcorp Genetics (formerly Invitae), LabCorp
552 conditions, 424 genes
Invitae Periodic Fever Syndromes Panel by Labcorp Genetics (formerly Invitae), LabCorp
32 conditions, 18 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.