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Results: 1 to 20 of 40

Tests names and labsConditionsGenes and analytesMethods

Gitelman syndrome

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

Bartter syndrome

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

Hypomagnesemia Sequencing Panel with CNV Detection

PreventionGenetics
United States
1616
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

ExomePLUS Electrolyte & Kidney Stone

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
4649
  • C Sequence analysis of the entire coding region

SLC12A3. Complete sequencing

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

Gitelman syndrome via the SLC12A3 Gene

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

Familial Hypomagnesemia , Panel Massive Sequencing (NGS) 14 Genes

Reference Laboratory Genetics
Spain
1614
  • C Sequence analysis of the entire coding region

Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes

Reference Laboratory Genetics
Spain
2122
  • C Sequence analysis of the entire coding region

Hereditary kidney disorders - different panels

Institute of Human Genetics Cologne University
Germany
28411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GITELMAN SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypomagnesemia (NGS panel for 17 genes)

CGC Genetics
Portugal
1717
  • C Sequence analysis of the entire coding region

Hypomagnesemia (NGS panel for 17 genes)

CGC Genetics
Portugal
1717
  • C Sequence analysis of the entire coding region

Gitelman Syndrome, Deletions-Duplications (MLPA) SLC12A3 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Gitelman Syndrome, Sequencing SLC12A3 Gene

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

Bartter syndrome

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis

Gitelman syndrome

LifeLabs Genetics
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter syndrome

LifeLabs Genetics
Canada
11
  • C Sequence analysis of the entire coding region

SLC12A3 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • C Sequence analysis of the entire coding region

Hypomagnesemia Panel

Blueprint Genetics
Finland
817
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BARTTER SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2927
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 40

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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