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Results: 1 to 20 of 27

Tests names and labsConditionsGenes and analytesMethods

Alport syndrome NGS panel

Connective Tissue Gene Tests
United States
14
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Alport syndrome Deletion/ Duplication panel

Connective Tissue Gene Tests
United States
14
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Alport syndrome Comprehensive panel

Connective Tissue Gene Tests
United States
14
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

KidneySeq - 264 Genes

Iowa Institute of Human Genetics University of Iowa
United States
102253
  • C Sequence analysis of the entire coding region

Alport syndrome panel

Collagen Diagnostic Laboratory University of Washington
United States
63
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Alport Syndrome (AS) Sequencing Panel

PreventionGenetics
United States
64
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

OtoGenome Test for Hearing Loss (110 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
23109
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Alport Syndrome (AS) via COL4A5 Gene Sequencing with CNV Detection

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Alport Syndrome (AS) via the COL4A4 Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Alport Syndrome (AS) via COL4A3 Gene Sequencing with CNV Detection

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

OtoSCOPE

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
181153
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Alport syndrome

Laboratory of Human Genetics GENOMED Health Care Center
Poland
13
  • 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

Comprehensive Hearing Loss and Deafness Panel

Blueprint Genetics
Finland
8179
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Alport Syndrome Panel

Blueprint Genetics
Finland
16
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Syndromic Hearing Loss Panel

Blueprint Genetics
Finland
686
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

KCNE5

Institute for Human Genetics University Clinic Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Inheritest NGS, Comprehensive

Integrated Genetics Westborough Integrated Genetics
United States
135140
  • T Targeted variant analysis

Inheritest NGS, Ashkenazi Jewish Ancestry Panel

Integrated Genetics Westborough Integrated Genetics
United States
3938
  • T Targeted variant analysis

Alport Syndrome, COL4A3-related

Integrated Genetics Westborough Integrated Genetics
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 27

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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