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Results: 1 to 20 of 23 (representing 4 labs)

Tests names and labsConditionsGenes and analytesMethods

Cancer NextGen Sequencing (NGS) and Deletion/Duplication Panel

PreventionGenetics
United States
4335
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Renal Cancer NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
2619
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Wilms Tumor via the WT1 Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GPC3

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

H19

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

WT1

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

BRCA2

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Renal/Kidney NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
7222
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer Syndrome: Sequencing Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
10645
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

X-linked Intellectual Disability: Gene Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
13991
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Disorders: Comprehensive Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
321207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

XLID NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
188107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Septo-optic Dysplasia NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
135
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

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

Lysosomal Disorders NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
193106
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
256112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
6825
  • -- Deletion/duplication analysis
  • -- Sequence analysis of the entire coding region

Epilepsy NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
598343
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Melanoma NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
7413
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pancreatic Cancer NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
4314
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 23

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.

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