t(7;19)(q34;q13)

**Semantic type:** Cell or Molecular Dysfunction

**Definition:** A chromosomal translocation involving breakpoints within the q34 band on the long arm of chromosome 7 and the q13 band on the long arm of chromosome 19. This rearrangement is associated with expression of either LSM14A-BRAF or CEP89-BRAF fusion genes and Spitzoid neoplasms.