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Results: 1 to 20 of 37

Tests names and labsConditionsGenes, analytes, and microbesMethods

Cancer Hotspot Panel

Centogene AG - the Rare Disease Company
Germany
4688
  • E Sequence analysis of select exons

Neuroblastoma, 256700, Autosomal dominant, Isolated cases (Neuroblastoma) (NME1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Neuroblastoma, susceptibility to, 1, 256700, Autosomal dominant, Isolated cases (Neuroblastoma) (KIF1B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Aventus GenSeq

Aventus Biolabs
United States
66133
  • C Sequence analysis of the entire coding region

Pediatric Cancer Panel

PreventionGenetics
United States
7864
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PrimBio Cancer HotSpot Panel

PrimBio Research Institute
United States
6050
  • T Targeted variant analysis

Neuroblastoma Panel

PreventionGenetics
United States
33
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cancer Panel

PreventionGenetics
United States
10999
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
843637
  • D Deletion/duplication analysis

Hereditary Neuroblastoma via the KIF1B Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Neuroblastoma (NGS panel based on disease exome of 3 genes)

CGC Genetics
Portugal
13
  • C Sequence analysis of the entire coding region

Clefting (WES based NGS panel of 231 genes, including CNV analysis)

CGC Genetics
Portugal
410231
  • C Sequence analysis of the entire coding region

Pheochromocytoma and paraganglioma (NGS panel of 17 genes)

CGC Genetics
Portugal
3617
  • C Sequence analysis of the entire coding region

Charcot-Marie-Tooth disease (NGS panel of 43 genes)

CGC Genetics
Portugal
9643
  • C Sequence analysis of the entire coding region

Neuroblastoma (sequence analysis of NME1 gene)

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

Broad Neuropathy Panel

LifeLabs Genetics
Canada
168175
  • C Sequence analysis of the entire coding region

Oxidative Phosphorylation Disorders NGS Panel

Fulgent Genetics
United States
416235
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuroblastoma , Panel Massive Sequencing (NGS) 4 Genes

Reference Laboratory Genetics
Spain
34
  • C Sequence analysis of the entire coding region

FISH - Solid Tumor

Warren G. Sanger Human Genetics Laboratory Nebraska Medicine (formerly a UNMC Lab)
United States
2241
  • F Fluorescence in situ hybridization (FISH)

Central Hypoventilation and Apnea Panel

Blueprint Genetics
Finland
415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 37

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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