Filters

Results: 1 to 14 of 14 (representing 5 labs)

Tests names and labsConditionsGenes and analytesMethods

CHD7 Sequence Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
41
  • T Targeted variant analysis

CHD7 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Genetics
United States
41
  • T Targeted variant analysis

CHD7 Sequence Analysis

Baylor Genetics
United States
41
  • C Sequence analysis of the entire coding region

CHD7 Deletion/Duplication Analysis (Prenatal Diagnosis)

Baylor Genetics
United States
41
  • D Deletion/duplication analysis

CHD7 Deletion/Duplication Analysis

Baylor Genetics
United States
41
  • D Deletion/duplication analysis

CHD7 Comprehensive - Sequence & Deletion/Duplication Analysis

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

Developmental Eye Disease panel

Molecular Vision Laboratory
United States
10959
  • C Sequence analysis of the entire coding region

CHD7

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

Endocrine Disorders: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
10857
  • C Sequence analysis of the entire coding region

Autism Panel: Tier 2

Emory Genetics Laboratory Emory University
United States
10360
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kallmann Syndrome NGS Panel

Fulgent Genetics
United States
2713
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Genetics
United States
177100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 14 of 14

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.

Support Center