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Results: 161 to 180 of 181

Tests names and labsConditionsGenes, analytes, and microbesMethods

CHD7 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypogonadotropic Hypogonadism (HH) and Related Disorders NGS Panel

Fulgent Genetics
United States
2213
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51334672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

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

Kallmann Syndrome NGS Panel

Fulgent Genetics
United States
2819
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
170106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARGE syndrome

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
672250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders/Rasopathies

Asper Biogene Asper Biogene LLC
Estonia
4536
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARGE syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARGE syndrome: CHD7 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

CHARGE Syndrome - CHD7 Known Point Mutation Analysis

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
11
  • T Targeted variant analysis

Gene Sequencing and generation of induced pluripotent stem cells

Donna M. Martin Laboratory University of Michigan
United States
11
  • T Targeted variant analysis

Severe Combined Immunodeficiency and T Cell Disorders Panel by next-generation sequencing (NGS)

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
3541
  • C Sequence analysis of the entire coding region

CHARGE Syndrome

Bioscientia GmbH Center for Human Genetics
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHARGE SYNDROME

Centre de Genetique Humaine Institut de Pathologie et de Genetique
Belgium
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CHD7-related disorders: CHD7 Sequencing

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Test for CHARGE Syndrome

Genome Diagnostics Laboratory The Hospital for Sick Children
Canada
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Charge Syndrome

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 161 to 180 of 181

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.