new paper: "A dataset of rare copy number variants associated with neurodevelopmental and neuropsychiatric disorders" https://doi.org/10.1038/s41597-026-07345-6
"We present a curated machine readable dataset, CNVPathwayAtlas, that integrates 38 pathogenic CNVs with their genomic coordinates, affected genes, molecular pathways, associated syndromes, and phenotypes. Each CNV is linked to a curated molecular pathway providing mechanistic insight into affected biological functions."










