Most other “pathogenic” and “likely pathogenic” CNVs do not overlap nor appear similar to CNVs listed in Decipher, but they do span “autism genes” listed in the SFARI GENE, and AutismKB databases, such as DMD, NEXMIF, NLGN4X, PRKN, and others (Table 2). The gene discussed is NEXMIF; the disease is autism.