ClinVar Genomic variation as it relates to human health

This CNV is a 196 kb deletion of 16p13.3, on chromosome 16, (seq[GRCh37]del(16)(p13.3); chr16:g.2635096_2830625del) which has been identified in a de novo state. This CNV constitutes a loss encompassing the following protein coding genes: ELOB, KCTD5, PDPK1, PRSS21, PRSS27, PRSS33, PRSS41, SRRM2, ZG16B, and partially overlaps the 16p13.3 microdeletion syndrome region. Mucha et al. (2019) reported eight individuals with overlapping deletions ranging from 205 kb to 504 kb in 16p13.3, and describe a minimal overlapping region encompassing three genes, TBC1D24, ATP6V0C, and PDPK1. At least six microdeletions were confirmed de novo. Common features of the syndrome included developmental delay, intellectual disability, and epilepsy. Additional features in these individuals included microcephaly, mildly dysmorphic features, hearing loss, strabismus, feeding difficulties, failure to thrive, short stature, behavioral problems including autism spectrum disorder, ADHD, and mania/bipolar episodes, and rarely an abnormal brain MRI. Additionally, in one individual with severe intellectual disability, epileptic seizures, skeletal abnormalities, and dysmorphic features, a de novo microdeletion at 16p13.3 involving TBC1D24 and ATP6V0C was reported (Kuroda et al. 2019). The CNV found in the proband overlaps at least six of the deletions reported in Mucha et al. (2019), but does not overlap the region of minimal overlap. This CNV has not been reported in controls. Based on the limited evidence currently available, this CNV is classified as a variant of uncertain significance.