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Results: 1 to 20 of 67

Tests names and labsConditionsGenes and analytesMethods

CentoICU platinum

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
769514
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

Rasopathies NGS Panel

Health in Code S.L.
Spain
2612
  • C Sequence analysis of the entire coding region

Expanded RASopathy Panel (14 Genes)

Laboratory for Molecular Medicine Partners HealthCare Personalized Medicine
United States
2014
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan syndrome type 7

Centogene AG - the Rare Disease Company
Germany
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

KRAS. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

NRAS. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

PTPN11. Sequencing of the exons 2, 3, 8, 9 and 13

Instituto de Medicina Genomica
Spain
61
  • E Sequence analysis of select exons

RAF1. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

RAF1. Sequencing of the exons 7, 14 and 17

Instituto de Medicina Genomica
Spain
61
  • E Sequence analysis of select exons

SOS1. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

SOS1. Sequencing of the exons 7, 11 and 17

Instituto de Medicina Genomica
Spain
61
  • E Sequence analysis of select exons

PTPN11. Complete sequencing

Instituto de Medicina Genomica
Spain
61
  • C Sequence analysis of the entire coding region

BRAF Sequence Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories
United States
41
  • T Targeted variant analysis

BRAF Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Miraca Genetics Laboratories
United States
41
  • T Targeted variant analysis

BRAF Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
41
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders/Rasopathies Sequencing Panel

PreventionGenetics
United States
2115
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Noonan Syndrome

Asper Biotech Asper Biotech Ltd.
Estonia
77
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 1 to 20 of 67

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.