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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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Anti-glomerular basement membrane disease
Synonyms: Anti-glomerular basement membrane antibody disease; Glomerulonephritis - pulmonary hemorrhage; Pulmonary renal syndrome; Rapidly progressive glomerulonephritis with pulmonary hemorrhage

Labs matching your search

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48 labs with tests matching your search
Lab name Tests matching your search
ARUP Laboratories, Molecular Genetics and Genomics United States1
Amsterdam UMC Genome Diagnostics Netherlands1
Athena Diagnostics United States2
Baylor Genetics United States8
Bioarray Spain1
Blueprint Genetics Finland4
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada1
CGC Genetics Portugal3
CGPP - Center for Predictive and Preventive Genetics Portugal2
CeGaT GmbH Germany3
Clinical Biochemical Genetics Diagnostic Laboratory United States2
Clinical Genomics Laboratory United States2
Clinical Genomics Unit Spain1
Collagen Diagnostic Laboratory United States1
DNA Labs India India1
Dhiti Omics Technologies Private Ltd India1
Dubai Health Genomic Medicine Center United Arab Emirates1
Duzen Laboratories Turkey1
Fulgent Genetics United States13
GeneDx United States8
GenepoweRx India1
Genome Diagnostics Laboratory Canada2
Genome-Nilou Lab Iran1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics United States2
Greenwood Genetic Center Diagnostic Laboratories United States1
HNL Genomics Connective Tissue Gene Tests United States9
Institute of Human Genetics Austria1
Integrated Genetics Westborough United States8
Intergen Genetics and Rare Diseases Diagnosis Center Turkey8
Johns Hopkins Genomics DNA Diagnostic Laboratory United States1
Knight Diagnostic Laboratories - Molecular Diagnostic Center United States1
Labcorp Genetics (formerly Invitae) United States5
Laboratorio de Genetica Clinica SL Spain7
Laboratory for Molecular Diagnostics Germany3
Laboratory for Molecular Medicine United States1
Laboratory of Human Genetics Poland1
MGZ Medical Genetics Center Germany1
MNG Laboratories (Medical Neurogenetics, LLC.) United States2
Machaon Diagnostics United States1
Mayo Clinic Laboratories United States4
Mendelics Brazil3
Molecular Otolaryngology and Renal Research Laboratories United States1
Molecular Vision Laboratory United States3
Myriad Genetics, Inc. United States1
Natera, Inc. United States9
Precision Medicine Care (PMC®) United States1
PreventionGenetics, part of Exact Sciences United States3
Variantyx, Inc. United States2
Results:
140 genetic tests from 48 labs with tests matching your search
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Download data for all or selected tests, using the check boxes in the search results to make your selection.
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51234672
  • 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

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

RenaDx™: Comprehensive Renal Disease Genetics Panel

Precision Medicine Care (PMC®)
United States
468448
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
United States
523337
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Deafness Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
405219
  • D Deletion/duplication analysis

OtoSCOPE v9

Molecular Otolaryngology and Renal Research Laboratories, University of Iowa Hospital and Clinics
United States
285218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Progressive Renal Disease Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
310195
  • D Deletion/duplication analysis

Targeted Variant Analysis

Integrated Genetics Westborough, LabCorp
United States
287578
  • 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
287578
  • D Deletion/duplication analysis
  • 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 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

Beacon Expanded Female Carrier Screening Plus Panel

Fulgent Genetics
United States
716335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Panel

Fulgent Genetics
United States
636298
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Male Carrier Screening Plus Panel

Fulgent Genetics
United States
661306
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beacon Expanded Female Carrier Screening Panel

Fulgent Genetics
United States
690326
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hearing Loss + mtDNA

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
218300
  • C Sequence analysis of the entire coding region

Hereditary Hearing Loss and Deafness Panel

PreventionGenetics, part of Exact Sciences
United States
364236
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
140 tests from 48 labs
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View the list of labs matching your search query.
More help
❮Page 1 of 7❯
Clinical Exome by Fulgent Genetics
5123 conditions, 4672 genes
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
Invitae Expanded Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
691 conditions, 388 genes
RenaDx™: Comprehensive Renal Disease Genetics Panel by Precision Medicine Care (PMC®)
468 conditions, 448 genes
RenalZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
523 conditions, 337 genes
Invitae Comprehensive Deafness Panel by Labcorp Genetics (formerly Invitae), LabCorp
405 conditions, 219 genes
OtoSCOPE v9 by Molecular Otolaryngology and Renal Research Laboratories, University of Iowa Hospital and Clinics
285 conditions, 218 genes
Invitae Progressive Renal Disease Panel by Labcorp Genetics (formerly Invitae), LabCorp
310 conditions, 195 genes
Targeted Variant Analysis by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes
Targeted Variant, Fetal Analysis by Integrated Genetics Westborough, LabCorp
292 conditions, 746 genes
GeneSeq PLUS by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes
GeneSeq PLUS, Fetal Analysis by Integrated Genetics Westborough, LabCorp
292 conditions, 597 genes
Partner Reflex to GeneSeq by Integrated Genetics Westborough, LabCorp
330 conditions, 746 genes
Inheritest 500 PLUS Panel by Integrated Genetics Westborough, LabCorp
287 conditions, 578 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Male Carrier Screening Panel by Fulgent Genetics
636 conditions, 298 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Comprehensive Hearing Loss + mtDNA by MNG Laboratories (Medical Neurogenetics, LLC.)
218 conditions, 300 genes
Hereditary Hearing Loss and Deafness Panel by PreventionGenetics, part of Exact Sciences
364 conditions, 236 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.