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Results: 21 to 38 of 38

Tests names and labsConditionsGenes, analytes, and microbesMethods

Nephrology Panel 

CGC Genetics Unilabs
Portugal
1334
  • C Sequence analysis of the entire coding region

Nephrotic Syndrome (sequence analyis of EMP2 gene)

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

Nephrotic Syndrome Panel

Mendelics
Brazil
149
  • C Sequence analysis of the entire coding region

NEPHROTIC SYNDROME EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
189
  • E Sequence analysis of select exons

Inherited Renal Disorders Panel

Dhiti Omics Technologies Private Ltd
India
7257
  • C Sequence analysis of the entire coding region

Nephrotic syndrome panel. 36-gene NGS panel.

Genologica Medica
Spain
4936
  • C Sequence analysis of the entire coding region

Nephrotic syndrome, type 10

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Nephrotic Syndrome/Focal Segmental Glomerulosclerosis

GeneDx
United States
355
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nephrotic syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2019
  • 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

Nephrotic Syndrome Panel

Blueprint Genetics
Finland
136
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nephrology Endocrinology and Electrolytes - panels

MGZ Medical Genetics Center
Germany
5117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EMP2 Single Gene

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

Nephrotic Syndrome and Focal and Segmental Glomerulosclerosis

Hildebrandt Laboratory Boston Children's Hospital
United States
261
  • C Sequence analysis of the entire coding region

Nephrotic Syndrome Panel

CeGaT GmbH
Germany
114
  • C Sequence analysis of the entire coding region

Nephrotic Syndrome and Focal Segmental Glomerulosclerosis panel

Clinical Genomics Laboratory Washington University in St. Louis
United States
1052
  • C Sequence analysis of the entire coding region

Hypoglycemia, Hyperinsulinism, Ketone Metabolism

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
242
  • C Sequence analysis of the entire coding region

Results: 21 to 38 of 38

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.