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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

SLC30A2 - NGS including CNV analysis

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

CentoICU Panel

Centogene AG - the Rare Disease Company
Germany
829848
  • C Sequence analysis of the entire coding region

Zinc deficiency, transient neonatal, 608118, Autosomal dominant; TNZD (SLC30A2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

ZINC DEFICIENCY IN BREAST MILK

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Zinc Deficiency in Breast Milk , Sequencing SLC30A2 Gene

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

Zinc deficiency, transient neonatal

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

SLC30A2 Single Gene

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

SLC30A2 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

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.