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t(19;22)(q13;q12)

MedGen UID:
1760790
Concept ID:
C5420798
Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the ZNF444 gene at 19q13 and the EWSR1 gene at 22q12. [from NCI]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVt(19;22)(q13;q12)

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