Last, Guasch et al.50report on a t(8;19)(p12;q13.3) translocation in an atypical stem‐cell myeloproliferative disorder, resulting in a HERV‐K LTR/fibroblast growth factor receptor 1 (FGFR1) fusion gene. The gene discussed is FGFR1; the disease is myeloproliferative disorder.