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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

HDAC8-histone deacetylase 8
Also know as: CDA07, CDLS5, HD8, HDACL1, KDAC8, MRXS6, RPD3, WTS; GeneID:55869; Location:Xq13.1;
Associated conditions: Cornelia de Lange syndrome 5;  De Lange syndrome

Labs matching your search

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29 labs with tests matching your search, 4 labs matching in other ways
Results:
100 genetic tests from 29 labs with tests matching your search, 4 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Microcephaly Panel

Genetic Services Laboratory, University of Chicago
United States
72133
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HDAC8 Gene Cornelia de Lange syndrome type 5 NGS Genetic DNA Test

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

Multigene panel for skeletal dysplasia based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1474
  • S Mutation scanning of the entire coding region

Multigene panel for autism spectrum disorders based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1163
  • S Mutation scanning 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

Invitae Neurodevelopmental Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
404241
  • D Deletion/duplication analysis

Invitae Limb and Digital Malformations Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
356177
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MarrowZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
United States
314230
  • C Sequence analysis of the entire coding region

Cornelia de Lange syndrome Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
55
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cornelia de Lange syndrome Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
55
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cornelia de Lange syndrome NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
55
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cornelia de Lange syndrome 5, 300882, X-linked dominant; CDLS5 (Cornelia de Lange syndrome) (HDAC8 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Cornelia de Lange syndrome 5, 300882, X-linked dominant; CDLS5 (Cornelia de Lange syndrome) (HDAC8 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

Epilepsy - Intellectual Disability - Autism Spectrum Disorder

Amplexa Genetics, Amplexa Genetics A/S
Denmark
1600
  • S Mutation scanning of the entire coding region

Cornelia de Lange syndrome NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
88
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cornelia de Lange syndrome Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
88
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cornelia de Lange syndrome Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
88
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Epilepsy Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
466297
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cornelia de Lange Syndrome and Related Disorders Panel

Labcorp Genetics (formerly Invitae), LabCorp
United States
4431
  • D Deletion/duplication analysis
100 tests from 29 labs
See all labs
View the list of labs matching your search query.
❮Page 1 of 5❯
Microcephaly Panel by Genetic Services Laboratory, University of Chicago
72 conditions, 133 genes
Multigene panel for skeletal dysplasia based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 474 genes
Multigene panel for autism spectrum disorders based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 163 genes
CentoNeuro Panel by CENTOGENE GmbH and LLC - Guiding Precision Medicine
1886 conditions, 1858 genes
Invitae Neurodevelopmental Disorders Panel by Labcorp Genetics (formerly Invitae), LabCorp
404 conditions, 241 genes
Invitae Limb and Digital Malformations Panel by Labcorp Genetics (formerly Invitae), LabCorp
356 conditions, 177 genes
MarrowZoom by Johns Hopkins Genomics DNA Diagnostic Laboratory, Johns Hopkins University, School of Medicine
314 conditions, 230 genes
Cornelia de Lange syndrome Comprehensive panel by HNL Genomics Connective Tissue Gene Tests
5 conditions, 5 genes
Cornelia de Lange syndrome NGS panel by HNL Genomics Connective Tissue Gene Tests
5 conditions, 5 genes
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
Cornelia de Lange syndrome NGS panel by HNL Genomics Connective Tissue Gene Tests
8 conditions, 8 genes
Cornelia de Lange syndrome Comprehensive panel by HNL Genomics Connective Tissue Gene Tests
8 conditions, 8 genes
Invitae Epilepsy Panel by Labcorp Genetics (formerly Invitae), LabCorp
466 conditions, 297 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.