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Results: 1 to 20 of 22 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel

Otogenetics
United States
124129
  • E Sequence analysis of select exons

Xeroderma Pigmentosum Sequencing Panel

PreventionGenetics
United States
108
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Xeroderma Pigmentosum via the ERCC3 Gene

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

Xeroderma pigmentosum group B (XPB, deletion/duplication analysis of ERCC3 gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Xeroderma pigmentosum group B (XPB, deletion/duplication analysis of ERCC3 gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

XERODERMA PIGMENTOSUM

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

ERCC3

Institute for Human Genetics University Clinic Freiburg
Germany
21
  • C Sequence analysis of the entire coding region

ONCOLOGY, PANEL

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
6780
  • C Sequence analysis of the entire coding region

CHOP Comprehensive Hereditary Cancer Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
92106
  • C Sequence analysis of the entire coding region

Progeria syndromes Panel

CeGaT GmbH
Germany
2018
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
174204
  • C Sequence analysis of the entire coding region

Xeroderma pigmentosum Panel

CeGaT GmbH
Germany
108
  • C Sequence analysis of the entire coding region

Disorders associated with malignancy Panel

CeGaT GmbH
Germany
2645
  • C Sequence analysis of the entire coding region

Trichothiodystrophy: ERCC3 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Cancer Predisposition

Asper Biogene Asper Biogene LLC
Estonia
12789
  • C Sequence analysis of the entire coding region

ERCC3

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Xeroderma Pigmentosum NGS Panel

Fulgent Genetics
United States
139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Xeroderma Pigmentosum NGS Panel

Fulgent Genetics
United States
117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hearing Loss NGS Panel

Fulgent Genetics
United States
202103
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
752392
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 22

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