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Results: 1 to 19 of 19

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Papillorenal syndrome

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

PAX2 sequencing

University of Minnesota Physicians Outreach Laboratory University of Minnesota
United States
21
  • C Sequence analysis of the entire coding region

ExomePLUS Cystic Disease & Dysplasia/Agenesis

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2122
  • C Sequence analysis of the entire coding region

Exome PLUS Proteinuria/FSGS & Hematuria

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2932
  • C Sequence analysis of the entire coding region

Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
3342
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PAX2. Complete sequencing

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

Renal Coloboma Syndrome and Isolated Renal Hypoplasia via the PAX2 Gene

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

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

PAX2 Gene Sequencing

GeneDx
United States
11
  • C Sequence analysis of the entire coding region

Renal-coloboma syndrome

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

Papillorenal syndrome (sequence analysis of PAX2 gene)

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

Developmental Eye Disease panel

Molecular Vision Laboratory
United States
8645
  • C Sequence analysis of the entire coding region

PAX2

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Disorders NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
252138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal Coloboma Syndrome (sequence analysis of PAX2 gene)

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

Papillorenal syndrome

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
21
  • C Sequence analysis of the entire coding region

Renal coloboma syndrome

Institute of Human Genetics Cologne University
Germany
11
  • C Sequence analysis of the entire coding region

Results: 1 to 19 of 19

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.