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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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Microcephaly 5, primary, autosomal recessive
Gene: ASPM

Labs matching your search

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41 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 States3
Ambry Genetics United States4
Athena Diagnostics United States5
Baylor Genetics United States5
Bioarray Spain1
CEN4GEN Institute for Genomics and Molecular Diagnostics Canada1
CENTOGENE GmbH and LLC - Guiding Precision Medicine Germany1
CGC Genetics Portugal1
CNH Molecular Diagnostics Laboratory United States8
CeGaT GmbH Germany5
Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory United States2
Clinical Genomics Laboratory United States1
DDC Clinic Molecular Diagnostics Laboratory United States1
Dhiti Omics Technologies Private Ltd India2
Fulgent Genetics United States56
Genesys Diagnostics United States5
Genetic Services Laboratory United States7
Genome Diagnostics Laboratory Netherlands1
Genome-Nilou Lab Iran1
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics United States3
Greenwood Genetic Center Diagnostic Laboratories United States3
HNL Genomics Connective Tissue Gene Tests United States9
Integrated Genetics Westborough United States9
Intergen Genetics and Rare Diseases Diagnosis Center Turkey52
Johns Hopkins Genomics DNA Diagnostic Laboratory United States3
Labcorp Genetics (formerly Invitae) United States33
Laboratorio de Genetica Clinica SL Spain2
MNG Laboratories (Medical Neurogenetics, LLC.) United States3
MVZ Dr. Eberhard & Partner Dortmund Germany2
Mayo Clinic Laboratories United States2
Molecular Diagnostic Laboratory United States1
Molecular Otolaryngology and Renal Research Laboratories United States1
Molecular Vision Laboratory United States4
Myriad Genetics, Inc. United States1
Natera, Inc. United States9
NxGen MDx United States2
Praxis fuer Humangenetik Wien Austria1
Precision Medicine Care (PMC®) United States1
PreventionGenetics, part of Exact Sciences United States29
Quantitative Genomic Medicine Laboratories, SL Spain1
Seattle Children's Hospital Genetics Laboratories United States3
Breakthrough Genomics United States0
Breda Genetics srl Italy0
DASA Brazil0
Victorian Clinical Genetics Services Australia0
Results:
284 genetic tests from 41 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.
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51284672
  • 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

MVL Vision Panel

Molecular Vision Laboratory
United States
16551199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

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 Leukodystrophy and Genetic Leukoencephalopathy Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
971680
  • D Deletion/duplication analysis

Invitae Inborn Errors of Immunity and Cytopenias Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
754562
  • D Deletion/duplication analysis

Invitae Comprehensive Deafness Panel

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

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

Invitae Cerebral Palsy Spectrum Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
638419
  • D Deletion/duplication analysis

Invitae Primary Immunodeficiency Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
552424
  • D Deletion/duplication analysis

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Invitae Skeletal Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
624349
  • D Deletion/duplication analysis

Comprehensive Primary Immunodeficiency NGS Panel

Fulgent Genetics
United States
1048472
  • D Deletion/duplication analysis
  • 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 Female Carrier Screening Panel

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

Comprehensive Hearing Loss NGS Panel

Fulgent Genetics
United States
332167
  • 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

Comprehensive Hearing Loss + mtDNA

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
218300
  • 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
284 tests from 41 labs
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View the list of labs matching your search query.
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❮Page 1 of 15❯
Clinical Exome by Fulgent Genetics
5128 conditions, 4672 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
MVL Vision Panel by Molecular Vision Laboratory
1655 conditions, 1199 genes
OtoSCOPE v9 by Molecular Otolaryngology and Renal Research Laboratories, University of Iowa Hospital and Clinics
285 conditions, 218 genes
Invitae Leukodystrophy and Genetic Leukoencephalopathy Panel by Labcorp Genetics (formerly Invitae), LabCorp
971 conditions, 680 genes
Invitae Inborn Errors of Immunity and Cytopenias Panel by Labcorp Genetics (formerly Invitae), LabCorp
754 conditions, 562 genes
Invitae Comprehensive Deafness Panel by Labcorp Genetics (formerly Invitae), LabCorp
405 conditions, 219 genes
Hereditary Hearing Loss and Deafness Panel by PreventionGenetics, part of Exact Sciences
364 conditions, 236 genes
Invitae Cerebral Palsy Spectrum Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
638 conditions, 419 genes
Invitae Primary Immunodeficiency Panel by Labcorp Genetics (formerly Invitae), LabCorp
552 conditions, 424 genes
Intellectual Disability NGS Panel by Fulgent Genetics
1058 conditions, 554 genes
MitoMet®Plus aCGH Analysis by Baylor Genetics
842 conditions, 637 genes
Invitae Skeletal Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
624 conditions, 349 genes
Comprehensive Primary Immunodeficiency NGS Panel by Fulgent Genetics
1048 conditions, 472 genes
Beacon Expanded Female Carrier Screening Plus Panel by Fulgent Genetics
716 conditions, 335 genes
Beacon Expanded Female Carrier Screening Panel by Fulgent Genetics
690 conditions, 326 genes
Comprehensive Hearing Loss NGS Panel by Fulgent Genetics
332 conditions, 167 genes
Beacon Expanded Male Carrier Screening Plus Panel by Fulgent Genetics
661 conditions, 306 genes
Comprehensive Hearing Loss + mtDNA by MNG Laboratories (Medical Neurogenetics, LLC.)
218 conditions, 300 genes
Beacon Expanded Male Carrier Screening Panel by Fulgent Genetics
636 conditions, 298 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.