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New filters have been added to narrow your search: Test target, to filter by number of genes; Genes and Conditions, to search by gene symbol or condition name; and Labs, to search by a laboratory name.

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Gene

ATP7B-ATPase copper transporting beta
Also know as: PWD, WC1, WD, WND; GeneID:540; Location:13q14.3;
Associated condition: Wilson disease

Labs matching your search

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61 labs with tests matching your search, 4 labs matching in other ways
Lab name Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States1
Amplexa Genetics Denmark1
Amsterdam UMC Genome Diagnostics Netherlands4
Baylor Genetics United States16
Bioarray Spain1
BloodGenetics Spain1
Blueprint Genetics Finland2
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada1
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany1
CGC Genetics Portugal11
CGPP - Center for Predictive and Preventive Genetics Portugal3
CeGaT GmbH Germany5
Center for Human Genetics Belgium1
Center for Human Genetics, Inc United States1
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States3
Clinical Biochemical Genetics Diagnostic Laboratory United States1
Codex Genetics Limited Hong Kong1
Color Diagnostics, LLC DBA Color Health United States1
DNA Labs India India1
Dhiti Omics Technologies Private Ltd India1
Diagenom GmbH Germany1
Duzen Laboratories Turkey2
Fulgent Genetics United States13
GeneDx United States11
Genesys Diagnostics United States1
Genetic Services Laboratory United States4
Genetics Service Unit India1
Genetiks Genetic Diagnosis Center Turkey1
Genome-Nilou Lab Iran1
HNL Genomics Connective Tissue Gene Tests United States3
Institute of Human Genetics Austria1
Institute of Medical Genetics and Genomics India1
Integrated Genetics Westborough United States10
Intergen Genetics and Rare Diseases Diagnosis Center Turkey2
Johns Hopkins Genomics DNA Diagnostic Laboratory United States1
Juno Genomics China1
Knight Diagnostic Laboratories - Molecular Diagnostic Center United States1
Labcorp Genetics (formerly Invitae) United States16
Labor Dr. Wisplinghoff Germany1
Laboratorio de Genetica Clinica SL Spain18
Laboratory of Human Genetics Poland1
MGZ Medical Genetics Center Germany2
MVZ Dr. Eberhard & Partner Dortmund Germany1
Mayo Clinic Laboratories United States4
Mendelics Brazil9
Molecular Diagnostics Laboratory South Korea1
Molecular Genetics Laboratory United States1
Molecular Vision Laboratory United States3
Myriad Genetics, Inc. United States1
Natera, Inc. United States9
National Taiwan University Hospital A1 Center Taiwan1
NxGen MDx United States2
OU Health Genetics Laboratory United States1
Praxis fuer Humangenetik Wien Austria1
Precision Medicine Care (PMC®) United States1
PreventionGenetics, part of Exact Sciences United States6
Quantitative Genomic Medicine Laboratories, SL Spain2
Tempus AI - CHI United States1
Tempus AI - RTP United States1
Translational Metabolic Laboratory Netherlands1
Variantyx, Inc. United States2
AiLife Diagnostics United States0
Breakthrough Genomics United States0
Dasa Brazil0
Victorian Clinical Genetics Services Australia0
Results:
198 genetic tests from 61 labs with tests matching your search, 4 labs matching in other ways
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Download data for all or selected tests, using the check boxes in the search results to make your selection.
 
Tests names and labsConditionsGenes, analytes, and microbesMethods

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
470449
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Carrier Screening - Comprehensive Panel (145 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
185145
  • D Deletion/duplication analysis
  • I Microsatellite instability testing (MSI)
  • X Mutation scanning of select exons
  • T Targeted variant analysis

ATP7B Gene Wilson disease NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Parkinson Disease Gene Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
194
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Nephrology Gene Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
1299
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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

Tempus xT

Tempus AI - CHI
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Wilson disease

Juno Genomics, Hangzhou Juno Genomics, Inc
China
11
  • C Sequence analysis of the entire coding region

NGS Panel for Iron related Anemias (including Aceruloplasminemia, Atransferrinemia, IRIDA, DMT1-deficiency =AHMIO1, Hypochromic microcytic anemia with iron overload 2=AHMIO2)

BloodGenetics
Spain
99
  • C Sequence analysis of the entire coding region

ATP7B gene sequencing

Molecular Genetics Laboratory, University of Michigan
United States
11
  • C Sequence analysis of the entire coding region

Wilson Disease Testing (ATP7B)

Genetic Services Laboratory, University of Chicago
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genetic test for Wilson disease (ATP7B gene)

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
11
  • S Mutation scanning of the entire coding region

Multigene panel for Parkinson’s disease and parkinsonism based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1106
  • S Mutation scanning of the entire coding region

Multigene panel for dystonias based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1257
  • S Mutation scanning of the entire coding region

Invitae Expanded Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
691388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Genomic Unity® Nuclear Encoded Mitochondrial Gene Analysis

Variantyx, Inc.
United States
1335
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

ATP7B Full Gene Analysis

Mayo Clinic Laboratories, Mayo Clinic
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
16541199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoNeuro Panel

CENTOGENE GmbH and LLC - Guiding Precision Medicine
Germany
18861858
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
198 tests from 61 labs
See all labs
View the list of labs matching your search query.
❮Page 1 of 10❯
Parkinson Disease Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 94 genes
Comprehensive Nephrology Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 299 genes
Renal Stone/Electrolyte Gene Panel by Mayo Clinic Laboratories, Mayo Clinic
82 conditions, 71 genes
Wilson disease by Juno Genomics, Hangzhou Juno Genomics, Inc
1 condition, 1 gene
ATP7B gene sequencing by Molecular Genetics Laboratory, University of Michigan
1 condition, 1 gene
Wilson Disease Testing (ATP7B) by Genetic Services Laboratory, University of Chicago
1 condition, 1 gene
Genetic test for Wilson disease (ATP7B gene) by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 1 gene
Multigene panel for Parkinson’s disease and parkinsonism based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 106 genes
Multigene panel for dystonias based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 257 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
691 conditions, 388 genes
ATP7B Full Gene Analysis by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 1 gene
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes

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.