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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Genetic Renal Panel v8

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
2117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical hemolytic uremic syndrome susceptibility and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical hemolytic uremic syndrome susceptibility and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atypical hemolytic uremic syndrome susceptibility and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Atypical hemolytic uremic syndrome susceptibility and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

aHUS/DDD Genetic Evaluation

Versiti Diagnostic Laboratories Versiti, Inc
United States
314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

C4BPA Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

Atypical Hemolytic Uremic Syndromes panel

Genetic Services Laboratory University of Chicago
United States
17
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Glomerular Proteinuria NGS Panel

Fulgent Genetics
United States
18276
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Thrombotic Microangiopathy NGS Panel

Fulgent Genetics
United States
5837
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Focus Thrombotic Microangiopathy NGS Panel

Fulgent Genetics
United States
4022
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary kidney disorders - different panels

Institute of Human Genetics Cologne University
Germany
32481
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Complement System Disorder Panel

Blueprint Genetics
Finland
175
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

C17orf67 Single Gene

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

DGKE Single Gene

Fulgent Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical hemolytic-uremic syndrome

Institute of Human Genetics Cologne University
Germany
98
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical Hemolytic Uremic Syndrome (aHUS) Genetic Susceptibility Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
518
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical Hemolytic-Uremic Syndrome Panel

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
113
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.