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Results: 1 to 20 of 22

Tests names and labsConditionsGenes and analytesMethods

Primary ciliary dyskinesia type 6

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

PulmoGene Panel (64 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
6664
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bronchiectasis Panel (17 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
1717
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Ciliary Dyskinesia (PCD) via the TXNDC3 Gene

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

Ciliopathy NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
9192
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Primary Ciliary Dyskinesia (PCD)/Immotile Cilia Syndrome Sequencing Panel

PreventionGenetics
United States
2832
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Heterotaxy, Situs Inversus and Kartagener's Syndrome Sequencing Panel

PreventionGenetics
United States
2931
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PRIMARY CILIARY DYSKINESIA

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1717
  • C Sequence analysis of the entire coding region

Single gene testing NME8

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Invitae Isolated and Syndromic Congenital Heart Disease Panel

Invitae
United States
10775
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliary dyskinesia, primary 6 (sequence analysis of NME8 gene)

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

Primary Ciliary Dyskinesia Panel

CeGaT GmbH
Germany
2934
  • C Sequence analysis of the entire coding region

NME8

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

Heterotaxy and Situs Inversus NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
2820
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kartagener's Syndrome or Heterotaxy with Chronic Respiratory Infections NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
1111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Primary Ciliary Dyskinesia Panel

Invitae
United States
3577
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pulmonary Disease: Comprehensive Sequencing Panel

Emory Genetics Laboratory Emory University
United States
7253
  • C Sequence analysis of the entire coding region

Bronchiectasis: Sequencing Panel

Emory Genetics Laboratory Emory University
United States
2016
  • C Sequence analysis of the entire coding region

Ciliopathies: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
165112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lung Disorders NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
8651
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 22

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.