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Results: 1 to 18 of 18 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

Bartter syndrome 4b

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

CLCNKA. Complete sequencing

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

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • 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

Bartter syndrome type 4B

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

Bartter syndrome type 4b (sequence analysis of CLCNKA gene)

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

qChip

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

CLCNKB Sequencing

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CLCNKB

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CLCNKA

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

Hereditary Renal Tubular Disorders Evaluation

Athena Diagnostics Inc
United States
65
  • C Sequence analysis of the entire coding region

CLCNKB DNA Sequencing Test

Athena Diagnostics Inc
United States
21
  • C Sequence analysis of the entire coding region

Epilepsy Advanced Sequencing Evaluation - Syndromic Disorders

Athena Diagnostics Inc
United States
2626
  • C Sequence analysis of the entire coding region

Epilepsy Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
143141
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
598343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

epiSEEK® Comprehensive Sequence Analysis for Epilepsy and Seizure Disorders

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
631431
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter syndrome, type 4b

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
12
  • C Sequence analysis of the entire coding region

Results: 1 to 18 of 18

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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