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Results: 1 to 20 of 32 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies

Mayo Clinic Genetic Testing Laboratories Mayo Clinic
United States
4140
  • C Sequence analysis of the entire coding region

Spherocytosis type 1

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

Spherocytosis panel

Centogene AG - the Rare Disease Company
Germany
15
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

NGS Panel for Hereditary hemolytic anemia including membranopathies (spherocytosis, elliptocytosis, xerocytosis, stomatocytosis, pyropoikylocytosis) and enzymopathies

BLOODGENETICS
Spain
3530
  • C Sequence analysis of the entire coding region

ANK1. Complete sequencing

Instituto de Medicina Genomica
Spain
51
  • C Sequence analysis of the entire coding region

Spherocytosis/Elliptocytosis Sequencing Panel

PreventionGenetics
United States
86
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Spherocytosis Type 1 via the ANK1 Gene

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hereditary Spherocytosis

Blood Cell Disease Reference Laboratory Yale University School of Medicine
United States
14
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Red Blood Cell Membrane Disorder Panel

Blueprint Genetics
Finland
35
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hematology Panel

Blueprint Genetics
Finland
4175
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Anemia Panel

Blueprint Genetics
Finland
268
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPHEROCYTOSIS

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
95
  • C Sequence analysis of the entire coding region

Erythrocytes, Anemia Panel

CeGaT GmbH
Germany
1433
  • C Sequence analysis of the entire coding region

Red Blood Cell Membrane Disorders Deletion/Duplication Panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
1412
  • D Deletion/duplication analysis

Hemolytic Anemia Deletion/Duplication Panel

Molecular Genetics Laboratory Cincinnati Children's Hospital Medical Center
United States
3232
  • D Deletion/duplication analysis

ANK1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • C Sequence analysis of the entire coding region

Hereditary spherocytosis type 1

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Hereditary Spherocytosis autosomal dominant only NGS panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
83
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 32

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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