WP_3Q29_COPY_NUMBER_VARIATION_SYNDROME
# https://www.gsea-msigdb.org/gsea/msigdb/human/geneset/WP_3Q29_COPY_NUMBER_VARIATION_SYNDROME
ADAM10
AKT1
BRINP1
CASP7
CEP19
CEP350
CEP43
DLG1
DYNC2H1
DYNC2I1
DYNC2I2
DYNC2LI1
DYNLL1
DYNLL2
DYNLRB1
DYNLRB2
DYNLT1
DYNLT2B
DYNLT3
FBXO45
FBXW7
FNDC8
GRIA1
HAMP
HFE
HIF1A
JUN
MAD2L1BP
MCRS1
MELTF
MYC
MYCBP2
NCBP1
NCBP2
NF2
NRROS
PAK2
PCYT1A
PIGM
PIGX
PIGZ
PIK3R3
PXN
RABL2B
RNF168
RNF8
SDHAP1
SENP5
SIRT1
SLC40A1
SLC51A
SLC51B
SMCO1
STAT5A
STAT5B
TF
TFRC
TGFB1
TM4SF19
UBE2N
UBXN7
WDR53
ZDHHC19
ZNF76