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t(1;19)(q10;p10)

MedGen UID:
476358
•Concept ID:
C3274725
•
Cell or Molecular Dysfunction

Definition

An unbalanced translocation between chromosomes 1 and 19. It is observed in oligodendrogliomas and results in the co-deletion of 1p and 19q. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(1;19)(q10;p10)

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