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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hyperoxaluria Panel, Random, Urine

Mayo Clinic Laboratories Mayo Clinic
United States
51
  • A Analyte

Renal Stone/Electrolyte Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Targeted Variant Analysis

Integrated Genetics Westborough LabCorp
United States
330746
  • T Targeted variant analysis

Targeted Variant, Fetal Analysis

Integrated Genetics Westborough LabCorp
United States
292746
  • T Targeted variant analysis

GeneSeq PLUS

Integrated Genetics Westborough LabCorp
United States
330746
  • C Sequence analysis of the entire coding region

GeneSeq PLUS, Fetal Analysis

Integrated Genetics Westborough LabCorp
United States
292597
  • C Sequence analysis of the entire coding region

Partner Reflex to GeneSeq

Integrated Genetics Westborough LabCorp
United States
330746
  • C Sequence analysis of the entire coding region

Inheritest 300 PLUS Panel

Integrated Genetics Westborough LabCorp
United States
172350
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Inheritest 500 PLUS Panel

Integrated Genetics Westborough LabCorp
United States
287578
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Inheritest High Frequency panel

Integrated Genetics Westborough LabCorp
United States
109110
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Inheritest 100 PLUS panel

Integrated Genetics Westborough LabCorp
United States
115142
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Peroxisomal Disorder Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
1726
  • C Sequence analysis of the entire coding region

Invitae Primary Hyperoxaluria Panel

Invitae
United States
43
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PRIMARY HYPEROXALURIA SANGER PANEL

Laboratorio de Genetica Clinica SL
Spain
13
  • 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

Hyperoxaluria Panel

CeGaT GmbH
Germany
43
  • C Sequence analysis of the entire coding region

Primary Hyperoxaluria (Type 1, Type 2, Type 3) Genetic Testing

Rare Kidney Stone Consortium And The Mayo Clinic Hyperoxaluria Center Mayo Clinic
United States
43
  • C Sequence analysis of the entire coding region

Hyperoxaluria, Primary, Type 3

Institute of Human Genetics Cologne University
Germany
21
  • C Sequence analysis of the entire coding region

Hyperoxaluria, Primary, Type 2

Institute of Human Genetics Cologne University
Germany
21
  • C Sequence analysis of the entire coding region

Hyperoxaluria, Primary, Type 1

Institute of Human Genetics Cologne University
Germany
21
  • 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.