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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

OnkoRisk Hereditary Oncology Management Panel

BioReference Health
United States
4717
  • C Sequence analysis of the entire coding region

OnkoRisk Hereditary Oncology Guideline Panel

BioReference Health
United States
7154
  • C Sequence analysis of the entire coding region

RNASEL - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prostate cancer 1, 601518, Autosomal dominant; HPC1 (Familial prostate cancer) (RNASEL 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

Prostate Cancer Panel

IntelligeneCG LLC
United States
314
  • C Sequence analysis of the entire coding region

Hereditary Disease Risk Test

Color Diagnostics, LLC DBA Color Health
United States
5159
  • C Sequence analysis of the entire coding region

Prostate Cancer NGS panel (germeline analysis)

CIBIC S.A.
Argentina
118
  • C Sequence analysis of the entire coding region

Prostate Cancer NGS panel (somatic analysis)

CIBIC S.A.
Argentina
118
  • C Sequence analysis of the entire coding region

Hereditary Prostate Cancer Panel

GeneDx
United States
2816
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Breast Cancer Management Panel

GeneDx
United States
249
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prostate Cancer

Asper Biogene Asper Biogene LLC
Estonia
2513
  • C Sequence analysis of the entire coding region

Familial Prostate Cancer , Panel Massive Sequencing (NGS) 11 Genes

Reference Laboratory Genetics
Spain
811
  • C Sequence analysis of the entire coding region

RNASEL Single Gene

Fulgent Genetics
United States
11
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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.