These 19 more variable repeat loci (RAI1, UMAD1, GLS, HTR7P1, CNKSR2, MAML3, MED15, MLLT3, USF3, MEF2A, MIR205HG, NCOR2, RPL14, JPH3, MAB21L1, ANKUB1, ERF, GIPC1, and EP400) were further screened in our ataxia patient cohort to identify any length variation that might be pathogenic (Fig. 3). The gene discussed is NCOR2; the disease is cerebellar ataxia.