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Results: 1 to 20 of 143

Tests names and labsConditionsGenes, analytes, and microbesMethods

NLRP3

Institute for Human Genetics University Medical Center Freiburg
Germany
41
  • C Sequence analysis of the entire coding region

NLRP3

Division of Human Genetics Medical University Innsbruck
Austria
31
  • S Mutation scanning of the entire coding region

NLRP3

Genome Diagnostics Laboratory University Medical Center Utrecht
Netherlands
21
  • C Sequence analysis of the entire coding region

NLRP3 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NLRP3 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

Cryopyrin-Associated Periodic Syndromes via the NLRP3 Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

NLRP3 - NGS including CNV analysis

Centogene US, LLC - The Rare Disease Company
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NLRP3 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CINCA syndrome, 607115, Autosomal dominant (CINCA syndrome) (NLRP3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

CINCA syndrome, 607115, Autosomal dominant (CINCA syndrome) (NLRP3 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Familial cold-induced inflammatory syndrome 1, 120100, Autosomal dominant; FCAS1 (Familial cold urticaria) (NLRP3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Muckle-Wells syndrome, 191900, Autosomal dominant; MWS (Muckle-Wells syndrome) (NLRP3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Muckle-Wells syndrome, 191900, Autosomal dominant; MWS (Muckle-Wells syndrome) (NLRP3 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

NLRP3. Complete sequencing

IGENOMIX
Spain
11
  • C Sequence analysis of the entire coding region

NLRP3. Complete sequencing

IGENOMIX
Spain
11
  • C Sequence analysis of the entire coding region

NLRP3/CIAS1. Complete sequencing

IGENOMIX
Spain
11
  • C Sequence analysis of the entire coding region

NLRP3/CIAS1. Complete sequencing

IGENOMIX
Spain
11
  • C Sequence analysis of the entire coding region

MEFV, TNFRSF1A, MVK, NLRP3. Complete sequencing by NGS

IGENOMIX
Spain
44
  • C Sequence analysis of the entire coding region

NLRP3. Complete sequencing

IGENOMIX
Spain
21
  • C Sequence analysis of the entire coding region

NLRP3 Exon 3 Sequencing

GeneDx
United States
41
  • E Sequence analysis of select exons

Results: 1 to 20 of 143

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.