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Variant : CV435473 (GRCh37/hg19 22q11.21-11.23(chr22:21798907-24963935)x3) Homo sapiens

Symbol: CV435473
Name: GRCh37/hg19 22q11.21-11.23(chr22:21798907-24963935)x3
Condition: See cases [RCV000510487]
Clinical Significance: uncertain significance
Last Evaluated: 02/14/2018
Review Status: no assertion criteria provided
Related Genes: ADORA2A   BCR   C22orf15   CABIN1   CCDC116   CHCHD10   DDT   DDTL   DERL3   DRICH1   GGT5   GGTLC2   GNAZ   GSTT1   GSTT2   GSTT2B   GUCD1   HIC2   IGLC1   IGLL1   IGLL5   MAPK1   MIF   MIR130B   MMP11   PPIL2   PPM1F   PPM1F-AS1   PRAME   RAB36   RGL4   RIMBP3C   RSPH14   SDF2L1   SLC2A11   SMARCB1   SNRPD3   SPECC1L   SUSD2   TMEM191C   TOP3B   UBE2L3   UPB1   VPREB1   VPREB3   YDJC   YPEL1   ZNF280A   ZNF280B   ZNF70  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh372221,798,907 - 24,963,935CLINVAR
Cytogenetic Map2222q11.21-11.23CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13443466
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-09-22
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.