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Results: 1 to 20 of 31

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

Bartter Syndrome panel

Centogene AG - the Rare Disease Company
Germany
127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter syndrome type 3

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

KidneySeq: A Comprehensive Inherited Kidney Disease Panel

Iowa Institute of Human Genetics University of Iowa
United States
122147
  • C Sequence analysis of the entire coding region

CLCNKB. Complete sequencing

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

Study of Molecular Markers Of Essential Hypertension and Associated Cardiovascular Events (35 genes - 57 genetic variants)

HeartGenetics IST spin-off community (Instituto Superior Técnico, Universidade de Lisboa)
Portugal
126
  • S Mutation scanning of the entire coding region
  • E Sequence analysis of select exons
  • T Targeted variant analysis

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

Comprehensive Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
3056447
  • 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 3: CLCNKB gene deletions-duplications analysis (MLPA)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • D Deletion/duplication analysis

Bartter syndrome type 3

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

Bartter Syndrome Panel

CeGaT GmbH
Germany
38
  • C Sequence analysis of the entire coding region

qChip

Quantitative Genomic Medicine Laboratories, SL
Spain
183162
  • 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

Hereditary Renal Tubular Disorders Evaluation

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

CLCNKB DNA Sequencing Test

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

Epilepsy Advanced Sequencing Evaluation - Syndromic Disorders

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

Epilepsy Advanced Sequencing Evaluation

Athena Diagnostics Inc Quest Diagnostics
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

Results: 1 to 20 of 31

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.