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t(6;22)(p21;q12)

MedGen UID:: 1726048
•Concept ID:: C5420801
•: Cell or Molecular Dysfunction

Definition

A chromosomal translocation involving the POU5F1 gene at 6p21 and the EWSR1 gene at 22q12. [from NCI]

Term Hierarchy

GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVt(6;22)(p21;q12)

Molecular Abnormality
- Cytogenetic Abnormality
  - Chromosomal Rearrangement
    - Gene Rearrangement Abnormality
      - EWSR1 Gene Rearrangement
        EWSR1 Gene Translocation
        t(6;22)(p21;q12)

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