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Results: 1 to 12 of 12

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

Hemolytic uremic syndrome, atypical, susceptibility to (sequence analysis of CFHR3 gene)

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

Hemolytic uremic syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
99
  • C Sequence analysis of the entire coding region

Comprehensive Glomerular Proteinuria NGS Panel

Fulgent Genetics
United States
18277
  • 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
1048473
  • 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

Dense Deposit Disease (DDD) and C3 Glomerulonephritis (C3GN) Gene Sequencing Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
58
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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

Test for DGKE-Related Atypical Hemolytic Uremic Syndrome

Secugen SL
Spain
81
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 12 of 12

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.