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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

NKX2-1 - Sanger sequencing

Centogene AG - the Rare Disease Company
Germany
31
  • C Sequence analysis of the entire coding region

Invitae Surfactant Metabolism Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
4019
  • D Deletion/duplication analysis

Invitae Neonatal Respiratory Distress Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
163111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Cerebral Palsy Spectrum Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
638419
  • D Deletion/duplication analysis

Neonatal Respiratory Distress Panel

PreventionGenetics, part of Exact Sciences
United States
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Thyroid cancer, monmedullary, 1, 188550, Autosomal dominant; NMTC1 (Differentiated thyroid carcinoma) (NKX2-1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Thyroid cancer, monmedullary, 1, 188550, Autosomal dominant; NMTC1 (Differentiated thyroid carcinoma) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

KRAS, BRAF, and NRA Mutation Analysis

PathGroup
United States
233
  • T Targeted variant analysis

BRAF and MSI Mutation Analysis

PathGroup
United States
151
  • I Microsatellite instability testing (MSI)
  • T Targeted variant analysis

KRAS, BRAF, NRAS and MSI Mutation Analysis

PathGroup
United States
233
  • T Targeted variant analysis

BRAF, NRAS, KIT Mutation Analysis

PathGroup
United States
163
  • T Targeted variant analysis

BRAF, EGFR, KRAS Mutation Analysis

PathGroup
United States
253
  • T Targeted variant analysis

Basic Lung Profile

PathGroup
United States
152
  • T Targeted variant analysis

PulmZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine
United States
171137
  • C Sequence analysis of the entire coding region

Panel of surfactant dysfunction and neonatal respiratory distress

Genologica Medica
Spain
75
  • C Sequence analysis of the entire coding region

Hypothyroidism and thyroid hormone resistance panel. NGS panel of 21 genes.

Genologica Medica
Spain
4221
  • C Sequence analysis of the entire coding region

Interstitial lung disease panel. 25-gene NGS panel.

Genologica Medica
Spain
4025
  • C Sequence analysis of the entire coding region

Complete panel of pulmonology. NGS panel of 66 genes.

Genologica Medica
Spain
11566
  • C Sequence analysis of the entire coding region

Lung Surfactant Deficiency. Panel NGS genes: ABCA3, FOXF1, NKX2-1, SFTPB, SFTPC.

Genologica Medica
Spain
75
  • C Sequence analysis of the entire coding region

Thyroid cancer, nonmedullary: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
47
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 20

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.