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Results: 1 to 20 of 35

Tests names and labsConditionsGenes and analytesMethods

Comprehensive pulmonary disease panel

Centogene AG - the Rare Disease Company
Germany
5766
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary ciliary dyskinesia type 11

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
6964
  • 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)/Immotile Cilia Syndrome Sequencing Panel with CNV Detection

PreventionGenetics
United States
3439
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Primary Ciliary Dyskinesia (PCD) via RSPH4A Gene Sequencing with CNV Detection

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

Ciliopathy Sequencing Panel with CNV Detection

PreventionGenetics
United States
9293
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Primary Ciliary Dyskinesia (PCD)/Immotile Cilia Syndrome and Cystic Fibrosis Sequencing Panel with CNV Detection

PreventionGenetics
United States
3440
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PCDNext

Ambry Genetics
United States
3021
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Ciliary Dyskinesia , Panel Massive Sequencing (NGS) 17 Genes

Reference Laboratory Genetics
Spain
1717
  • C Sequence analysis of the entire coding region

Ciliopathies: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
14196
  • D Deletion/duplication analysis

Bronchiectasis: Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
2016
  • D Deletion/duplication analysis

Primary Ciliary Dyskinesia and Cystic Fibrosis Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4142
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
9293
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary-Vascular Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
5964
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary Ciliary Dyskinesia Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
3137
  • D Deletion/duplication analysis

Comprehensive Pulmonary-Vascular Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
5964
  • D Deletion/duplication analysis

Comprehensive Pulmonary-Vascular Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
6065
  • C Sequence analysis of the entire coding region

Primary Ciliary Dyskinesia Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
3237
  • C Sequence analysis of the entire coding region

Primary Ciliary Dyskinesia Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
3137
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 35

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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