Filters

See more specimen types...

Other countries

Results: 1 to 20 of 31

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

11 beta hydroxylase

Clinical Biochemistry Laboratory UCL Hospitals
United Kingdom
11
  • C Sequence analysis of the entire coding region

Adrenal hyperplasia, congenital, due to steroid 11-beta-hydroxylase deficiency

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

CYP11B1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • 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
844637
  • D Deletion/duplication analysis

nucSEEK® Comprehensive Sequence Analysis Of The Nuclear Mitochondrial Exome

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
560420
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia: Steroid Profile, Quantitative, Dried Blood Spot

Emory Genetics Laboratory Emory University
United States
35
  • A Analyte

Abnormal/Ambiguous Genitalia Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
8272
  • C Sequence analysis of the entire coding region

CarrierMap

Recombine
United States
299297
  • T Targeted variant analysis

CYP11B1

Division Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

CYP11B1

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

Monogenic Hypertension Evaluation

Athena Diagnostics Inc Quest Diagnostics
United States
44
  • C Sequence analysis of the entire coding region

CYP11B1 DNA Sequencing Test

Athena Diagnostics Inc Quest Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia (CAH) Evaluation

Athena Diagnostics Inc Quest Diagnostics
United States
22
  • C Sequence analysis of the entire coding region

CYP11B1 (CAH) DNA Sequencing Test

Athena Diagnostics Inc Quest Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

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

Results: 1 to 20 of 31

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.