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Results: 1 to 20 of 75

Tests names and labsConditionsGenes, analytes, and microbesMethods

Red Blood Cell Membrane Panel, Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
1914
  • C Sequence analysis of the entire coding region

Red Blood Cell Enzyme Panel, Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
1917
  • C Sequence analysis of the entire coding region

Congenital Dyserythropoietic Anemia Panel, Next-Generation Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
610
  • C Sequence analysis of the entire coding region

UDP-Glucuronosyl Transferase 1A1 (UGT1A1), Full Gene Sequencing

Mayo Clinic Laboratories Mayo Clinic
United States
111
  • C Sequence analysis of the entire coding region

Gilbert syndrome (UGT1A1 gene)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
13
  • T Targeted variant analysis

UGT1A1 genotyping for Gilbert Syndrome

Genetic Services Laboratory University of Chicago
United States
11
  • T Targeted variant analysis

UGT1A1 - NGS including CNV analysis

Centogene US, LLC - The Rare Disease Company
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

UGT1A1 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Pharmacogenomics Panel

Invitae
United States
4337
  • T Targeted variant analysis

Invitae Crigler Najjar and Gilbert Syndrome Test

Invitae
United States
51
  • D Deletion/duplication analysis

Invitae Cholestasis Panel

Invitae
United States
210134
  • D Deletion/duplication analysis

Congenital Anomalies of the Gastrointestinal Tract Panel

PreventionGenetics
United States
297180
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Cholestasis Panel

PreventionGenetics
United States
13069
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

[Gilbert syndrome], 143500, Autosomal recessive (UGT1A1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

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

UGT1A1 Genotyping

IU Genetic Testing Laboratories Indiana University School of Medicine
United States
11
  • T Targeted variant analysis

Gilbert syndrome Genotyping

IU Genetic Testing Laboratories Indiana University School of Medicine
United States
11
  • T Targeted variant analysis

Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene

PreventionGenetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

UGT1A1. Detection of the allele A(TA)7TAA in promotor region by real time PCR

IGENOMIX
Spain
11
  • T Targeted variant analysis

UGT1A1. Complete sequencing

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

Cholestasis panel. NGS panel of 46 genes.

Genologica Medica
Spain
8846
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 75

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.