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Results: 1 to 20 of 159

Tests names and labsConditionsGenes, analytes, and microbesMethods

MVK

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

MVK

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

MVK

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

MVK Gene Porokeratosis type 3, disseminated superficial actinic NGS Genetic DNA Test

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

MVK Gene Mevalonic aciduria NGS Genetic DNA Test

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

MVK Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVK Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
31
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hyper IgD Syndrome/Mevalonate Aciduria via the MVK Gene

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

MVK - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyper-IgD syndrome, 260920, Autosomal recessive; HIDS (Hyperimmunoglobulinemia D with periodic fever) (MVK 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

Hyper-IgD syndrome, 260920, Autosomal recessive; HIDS (Hyperimmunoglobulinemia D with periodic fever) (MVK gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Mevalonic aciduria, 610377, Autosomal recessive; MEVA (Mevalonic aciduria) (MVK 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

Mevalonic aciduria, 610377, Autosomal recessive; MEVA (Mevalonic aciduria) (MVK gene) (Sequence Analysis-All Coding Exons) (Prenatal)

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

Porokeratosis 3, multiple types, 175900, Autosomal dominant; POROK3 (Porokeratosis of Mibelli) (MVK 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

MVK Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hiper IgD syndrome (sequence analysis of MVK gene)

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

Hyper IgD Syndrome (deletion/duplication analysis of MVK gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

Mevalonate Kinase Deficiency (MVK Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyper IgD and Periodic Fever Syndrome, Sequencing Exons (2,9,11) MVK Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Hyper IgD and Periodic Fever Syndrome, Sequencing MVK Gene

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

Results: 1 to 20 of 159

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.