Filters

See more specimen types...
See more states

Other countries

Results: 1 to 20 of 52 (representing 22 labs)

Tests names and labsConditionsGenes and analytesMethods

Congenital heart defects panel

Centogene AG - the Rare Disease Company
Germany
2612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive SCID panel

Centogene AG - the Rare Disease Company
Germany
2523
  • C Sequence analysis of the entire coding region

B-positive SCID panel

Centogene AG - the Rare Disease Company
Germany
1615
  • C Sequence analysis of the entire coding region

AllNeuro panel

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

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

DiGeorge syndrome

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

Congenital heart diseases Panel

Health in Code S.L.
Spain
176
  • C Sequence analysis of the entire coding region

Cardiovascular Diseases_General Panel

Health in Code S.L.
Spain
1380
  • C Sequence analysis of the entire coding region

TBX1. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Congenital Heart Diseases Panel

Health in Code S.L.
Spain
139
  • C Sequence analysis of the entire coding region

Cardiomyopathies Panel

Health in Code S.L.
Spain
1149
  • C Sequence analysis of the entire coding region

Inherited Cardiovascular Diseases and Sudden Death Panel

Health in Code S.L.
Spain
1213
  • C Sequence analysis of the entire coding region

Congenital Heart Disease Panel

Heart Institute Diagnostic Lab Cincinnati Children's Hospital Medical Center
United States
13
  • S Mutation scanning of the entire coding region

TBX1 Sequencing

Heart Institute Diagnostic Lab Cincinnati Children's Hospital Medical Center
United States
11
  • S Mutation scanning of the entire coding region

OtoSCOPE

Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics
United States
98147
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Severe combined immunodeficiency Del/dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1718
  • D Deletion/duplication analysis

Severe combined immunodeficency Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1718
  • C Sequence analysis of the entire coding region

Severe combined immunodeficiency Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1718
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypoparathyroidism sequencing panel

Genetic Services Laboratory University of Chicago
United States
2117
  • C Sequence analysis of the entire coding region

Severe Combined Immunodeficiency Panel

Blueprint Genetics
Finland
168
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 52

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.

Support Center