Human Gene Set: WP_16P122_COPY_NUMBER_VARIATION_SYNDROME_520KB


Standard name WP_16P122_COPY_NUMBER_VARIATION_SYNDROME_520KB
Systematic name M49233
Brief description 16p12.2 copy number variation syndrome (520kb)
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP5510
Related gene sets  
External links https://www.wikipathways.org/pathways/WP5510
Filtered by similarity ?
Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
Download gene set format: grp | gmt | xml | json | TSV metadata
Compute overlaps ? (show collections to investigate for overlap with this gene set)
Compendia expression profiles ? NG-CHM interactive heatmaps
(Please note that clustering takes a few seconds)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)

Legacy heatmaps (PNG)
GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 54 genes
Gene families ? Categorize these 54 genes by gene family
Show members (show 54 source identifiers mapped to 54 genes)
Version history 2025.1.Hs: First Introduced.

See MSigDB license terms here. Please note that certain gene sets have special access terms.