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Results: 21 to 40 of 47

Tests names and labsConditionsGenes, analytes, and microbesMethods

Disorders of Copper Metabolism Panel

PreventionGenetics, part of Exact Sciences
United States
96
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Mendelian Disorders with Psychiatric Symptoms Panel

Invitae
United States
247163
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

WES iron disorders

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
2046
  • E Sequence analysis of select exons

panel microcytic anemia-due to iron disorder (SLC11A2, TMPRSS6, TF, CP)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
44
  • C Sequence analysis of the entire coding region

CP - hereditary hypoceruloplasminemia

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

panel hemochromatosis (CP, HFE, HFE2, HAMP, TFR2, SLC40A1, BMP6, FTL, IRE-FTH1)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
89
  • C Sequence analysis of the entire coding region

Parkinson Disease and Parkinsonism Panel

PreventionGenetics, part of Exact Sciences
United States
6870
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Treatable Neurometabolic Disorders Panel

Invitae
United States
257191
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Copper Metabolism Disorders Panel

Invitae
United States
1510
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurodegeneration with Brain Iron Accumulation and Infantile Neuroaxonal Dystrophy Panel

PreventionGenetics, part of Exact Sciences
United States
1816
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Aceruloplasminemia via the CP Gene

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

Ataxia panel. NGS panel of 157 genes.

Genologica Medica
Spain
247156
  • C Sequence analysis of the entire coding region

CP gene sequencing

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Aceruloplasminemia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Aceruloplasminemia (CP Single Gene Test)

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

Brain-Iron Accumulation NGS Panel

Fulgent Genetics
United States
3613
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACERULOPLASMINEMIA

Laboratorio de Genetica Clinica SL
Spain
11
  • 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

Aceruloplasminemia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing CP

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

Results: 21 to 40 of 47

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.