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Results: 1 to 12 of 12

Tests names and labsConditionsGenes and analytesMethods

Erythrocytosis, familial type 3

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

NGS Panel for Congenital Erythrocythosis or Familiar Polycythemia

BLOODGENETICS
Spain
44
  • C Sequence analysis of the entire coding region

Pheochromocytoma and paraganglioma (NGS panel for 16 genes)

CGC Genetics
Portugal
1016
  • C Sequence analysis of the entire coding region

Pheochromocytoma and paraganglioma (NGS panel for 16 genes)

CGC Genetics
Portugal
1016
  • C Sequence analysis of the entire coding region

POLYCYTHEMIA, SECONDARY (AUTOSOMAL DOMINANT)

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

Familial Erythrocytosis, Sequencing EGLN1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Erythrocytosis, Familial: EGLN1 gene sequence analysis

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

Erythrocytosis, Familial: EGLN1 gene sequence analysis

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

Erythrocytosis familial, 3 (sequence analysis of EGLN1 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

EGLN1

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paraganglioma-Pheochromocytomas NGS Panel

Fulgent Genetics
United States
3412
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Cancer NGS Panel

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

Results: 1 to 12 of 12

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