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Variant : CV435680 (GRCh37/hg19 Xp11.21-q21.1(chrX:55240087-78225374)x1) Homo sapiens

Symbol: CV435680
Name: GRCh37/hg19 Xp11.21-q21.1(chrX:55240087-78225374)x1
Condition: See cases [RCV000511311]
Clinical Significance: pathogenic
Last Evaluated: 02/16/2015
Review Status: no assertion criteria provided
Related Genes: ABCB7   AMER1   AR   ARHGEF9   ARR3   ASB12   ATP7A   ATRX   AWAT1   AWAT2   CDX4   CHIC1   CITED1   COX7B   CXCR3   CXorf49   CXorf49B   CXorf65   CYSLTR1   DGAT2L6   DLG3   DMRTC1   DMRTC1B   EDA   EDA2R   EFNB1   ERCC6L   FAAH2   FAM155B   FGF16   FOXO4   FOXR2   FTX   GCNA   GDPD2   GJB1   HDAC8   HEPH   IGBP1   IL2RG   ITGB1BP2   JPX   KIF4A   KLF8   LAS1L   LPAR4   MAGEE1   MAGEE2   MAGEH1   MAGT1   MED12   MIR223   MSN   MTMR8   NAP1L2   NEXMIF   NHSL2   NLGN3   NONO   OGT   OPHN1   OTUD6A   P2RY10   P2RY4   PABPC1L2A   PABPC1L2B   PAGE3   PAGE5   PBDC1   PDZD11   PGAM4   PGK1   PHKA1   PIN4   PJA1   RAB41   RLIM   RPS4X   RRAGB   RTL3   RTL5   SLC16A2   SLC7A3   SNX12   SPIN2A   SPIN2B   SPIN3   SPIN4   STARD8   TAF1   TAF9B   TEX11   TSIX   UBQLN2   UPRT   USP51   VSIG4   XIST   YIPF6   ZC3H12B   ZC4H2   ZCCHC13   ZDHHC15   ZMYM3   ZXDA   ZXDB  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X55,240,087 - 78,225,374CLINVAR
Cytogenetic MapXXp11.21-q21.1CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13444284
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE


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