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Results: 1 to 20 of 24

Tests names and labsConditionsGenes, analytes, and microbesMethods

Genomind Pharmacogenetic Report

Genomind, Inc. Genomind, Inc
United States
1427
  • T Targeted variant analysis

Methylation analysis for Prader Willi / Angelman Syndrome

GENETIX Centro de Investigación en Genética Humana y Reproductiva
Colombia
71
  • M Methylation analysis

SLC6A4 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Memory impairment, susceptibility to (BDNF gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Obsessive-compulsive disorder, protection against, 164230, Autosomal dominant (BDNF gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Obsessive-compulsive disorder, susceptibility to, 164230, Autosomal dominant; OCD (HTR2A gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Obsessive-compulsive disorder, 164230, Autosomal dominant (SLC6A4 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

Huntington Disease Repeat Expansion Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
31
  • T Targeted variant analysis

Huntington Disease Repeat Expansion Analysis

Baylor Genetics
United States
31
  • T Targeted variant analysis

SLC6A4 Full Gene Sequencing Analysis

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
21
  • C Sequence analysis of the entire coding region

Neurotransmitter Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
85101
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism Spectrum Disorders (Expanded Panel) , Panel Massive Sequencing (NGS) 77 Genes

Reference Laboratory Genetics
Spain
8577
  • C Sequence analysis of the entire coding region

Rett Syndrome and Related Disorders , Panel Massive Sequencing (NGS) 18 Genes

Reference Laboratory Genetics
Spain
1718
  • C Sequence analysis of the entire coding region

BDNF Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SLC6A4 Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HTR2A Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BDNF Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Serotonin Metabolism Deficiency NGS Panel

Fulgent Genetics
United States
1217
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Central Hypoventilation Syndrome NGS Panel

Fulgent Genetics
United States
146
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 24

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.