In humans, it has been reported that multiple types of heterozygous genomic structural variants in the AUTS2 locus including de novo balanced translocation, inversion, or intragenic deletions are associated with a wide range of psychiatric illnesses such as ASDs, ID, ADHD, schizophrenia, and dyslexia, as well as other neuropsychiatric diseases (Oksenberg and Ahituv, 2013). Here, AUTS2 is linked to dyslexia.