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Results: 1 to 20 of 214

Tests names and labsConditionsGenes, analytes, and microbesMethods

T-cell acute lymphoblastic leukemia, somatic, 613065 (Acute lymphoblastic leukemia) (BAX 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

Leukemia, acute lymphoblastic, 613065 (Nijmegen breakage syndrome) (NBN 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

Leukemia, T-cell acute lymphoblastic, somatic, 613065 (Acute lymphoblastic leukemia) (NUP214 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

Leukemia, T-cell acute lymphocytic, somatic, 613065 (Acute lymphoblastic leukemia) (TAL2 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

Leukemia, acute lymphoblastic, somatic, 613065 (Acute lymphoblastic leukemia) (FLT3 gene) (Sequence Analysis) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • E Sequence analysis of select exons

Leukemia, T-cell acute lymphocytic, somatic, 613065 (Acute lymphoblastic leukemia) (TAL1 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

Leukemia, acute lymphoblastic, somatic, 613065 (Acute lymphoblastic leukemia) (GNB1 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

Pipecolic Acid, S

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • A Analyte

Quantitative Chimerism

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • T Targeted variant analysis

PREVENTEST

GeneID Lab - Advanced Molecular Diagnostics
United States
6034
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bone marrow culture for cancer

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
424
  • K Karyotyping

BCR/ABL, p210, MRNA Detection Monitoring

Sanford Medical Genetics Laboratory Sanfordhealth
United States
22
  • T Targeted variant analysis

clonoSEQ®

Adaptive Biotechnologies
United States
53
  • E Sequence analysis of select exons

Comprehensive HemeComplete Profile + Heme Fusion + CALR PCR + FLT3 PCR

PathGroup
United States
16160
  • T Targeted variant analysis

CentoBreast

Centogene AG - the Rare Disease Company
Germany
5828
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoColon

Centogene AG - the Rare Disease Company
Germany
6733
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoCancer

Centogene AG - the Rare Disease Company
Germany
11368
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CentoCancer Comprehensive

Centogene AG - the Rare Disease Company
Germany
155107
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Solid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
218135
  • C Sequence analysis of the entire coding region

Myeloid Tumor Panel

Centogene AG - the Rare Disease Company
Germany
7434
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 214

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.