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Results: 1 to 20 of 23

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

qGenEx Sex development disorders

Quantitative Genomic Medicine Laboratories, SL
Spain
4548
  • C Sequence analysis of the entire coding region

CYP11B1 Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • C Sequence analysis of the entire coding region

CYP11B1 Prenatal Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • E Sequence analysis of select exons

CYP11B1 Familial Mutation/Variant Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • E Sequence analysis of select exons

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Hereditary kidney disorders - different panels

Institute of Human Genetics Cologne University
Germany
28411
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FAMILIAL HYPERALDOSTERONISM TYPE 1, GLUCOCORTICOID REMEDIABLE ALDOSTERONISM

Laboratorio de Genetica Clinica SL
Spain
12
  • T Targeted variant analysis

CYP11B1 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
52
  • C Sequence analysis of the entire coding region

Familial hyperaldosteronism type 1

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

CYP11B1

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

CYP11B1/2 DNA Chimeric Gene Fusion Test

Athena Diagnostics Inc
United States
12
  • T Targeted variant analysis

Familial hyperaldosteronism type 1 (sequence analysis of CYP11B2 gene)

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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
601504
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Aldosteronism, glucocorticoid-remediable

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Aldosteronism, glucocorticoid-remediable

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Glucocorticoid-remediable aldosteronism: Fusion of CYP11B1 and CYP11B2 genes

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
12
  • C Sequence analysis of the entire coding region

Glucocorticoid-remediable Aldosteronism

Human Genetics Ruhr University
Germany
11
  • D Deletion/duplication analysis

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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