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Results: 1 to 20 of 24 (representing 17 labs)

Tests names and labsConditionsGenes and analytesMethods

NBIA Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
910
  • C Sequence analysis of the entire coding region

NBIA Deletion/Duplication Analysis

Genetic Services Laboratory University of Chicago
United States
1010
  • D Deletion/duplication analysis

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Neurodegeneration with brain iron accumulation 4

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

Mitochondrial Membrane Protein-Associated Neurodegeneration via the C19orf12 Gene

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

Neurodegeneration with Brain Iron Accumulation and Infantile Neuroaxonal Dystrophy Sequencing Panel

PreventionGenetics
United States
1211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

NEURODEGENERATION WITH BRAIN IRON ACCUMULATION (NBIA): NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
99
  • C Sequence analysis of the entire coding region

Neurodegeneration with brain iron accumulation (NGS panel of 8 genes)

CGC Genetics
Portugal
88
  • C Sequence analysis of the entire coding region

Neurodegeneration with brain iron accumulation (NGS panel of 8 genes)

CGC Genetics
Portugal
88
  • C Sequence analysis of the entire coding region

Neurodegeneration with Brain Iron Accumulation Type 4 , Sequencing C19orf12 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
351275
  • C Sequence analysis of the entire coding region

Invitae Neurodegeneration with Brain Iron Accumulation Panel

Invitae
United States
1611
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurodegeneration with Brain Iron Accumulation

Asper Biogene Asper Biogene LLC
Estonia
1010
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegia Spotlight Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
8658
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

C19ORF12 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
21
  • C Sequence analysis of the entire coding region

Neurodegeneration with Brain Iron Accumulation Disorders

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
129
  • C Sequence analysis of the entire coding region

NGS panel - Neurodegeneration with brain iron accumulation

Genome Diagnostics VU University Medical Center
Netherlands
1110
  • S Mutation scanning of the entire coding region
  • T Targeted variant analysis

Neurodegeneration with Brain Iron Accumulation NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
179
  • C Sequence analysis of the entire coding region

Hereditary spastic paraplegia (NGS panel for 43 genes)

CGC Genetics
Portugal
4043
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 24

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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