Human Gene Set: WP_17Q12_COPY_NUMBER_VARIATION_SYNDROME


Standard name WP_17Q12_COPY_NUMBER_VARIATION_SYNDROME
Systematic name M46448
Brief description 17q12 copy number variation syndrome
Full description or abstract  
Collection C2: Curated
      CP: Canonical Pathways
            CP:WIKIPATHWAYS: WikiPathways
Source publication  
Exact source WP5287
Related gene sets  
External links https://www.wikipathways.org/pathways/WP5287
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Source species Homo sapiens
Contributed by WikiPathways
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
Dataset references  
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Version history 2024.1.Hs: Updated to WikiPathways Release 20240710

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