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Variant : CV383092 (GRCh37/hg19 Xq26.3-28(chrX:134114063-155233731)x1) Homo sapiens

Symbol: CV383092
Name: GRCh37/hg19 Xq26.3-28(chrX:134114063-155233731)x1
Condition: See cases [RCV000448865]
Clinical Significance: pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ABCD1   ADGRG4   AFF2   ARHGAP4   ARHGEF6   ATP11C   ATP2B3   ATP6AP1   AVPR2   BCAP31   BGN   BRCC3   BRS3   CCNQ   CD40LG   CD99L2   CDR1   CETN2   CLIC2   CMC4   CNGA2   CSAG1   CSAG3   CT45A1   CT45A2   CT45A3   CT45A5   CT45A6   CT55   CTAG1A   CTAG1B   CTAG2   CXorf51A   CXorf51B   CXorf66   DKC1   DNASE1L1   DUSP9   EMD   EOLA1   EOLA2   F8   F8A1   F8A2   F8A3   F9   FAM3A   FAM50A   FATE1   FGF13   FHL1   FLNA   FMR1   FMR1-AS1   FMR1NB   FUNDC2   G6PD   GAB3   GABRA3   GABRE   GABRQ   GDI1   GPR101   GPR50   GPR50-AS1   H2AB1   H2AB2   H2AB3   HAUS7   HCFC1   HMGB3   HSFX1   HSFX2   HTATSF1   IDH3G   IDS   IKBKG   INTS6L   IRAK1   L1CAM   LAGE3   LDOC1   MAGEA1   MAGEA10   MAGEA11   MAGEA12   MAGEA2   MAGEA2B   MAGEA3   MAGEA4   MAGEA5   MAGEA6   MAGEA8   MAGEA9   MAGEA9B   MAGEC1   MAGEC2   MAGEC3   MAMLD1   MAP7D3   MCF2   MECP2   MIR105-1   MIR105-2   MIR224   MIR506   MIR508   MIR509-1   MIR509-3   MIR510   MMGT1   MPP1   MTCP1   MTM1   MTMR1   NAA10   NSDHL   OPN1LW   OPN1MW   OPN1MW2   PASD1   PDZD4   PLXNA3   PLXNB3   PNCK   PNMA3   PNMA5   PNMA6A   PNMA6E   PRRG3   RAB39B   RBMX   RENBP   RPL10   RTL8A   RTL8B   RTL8C   SAGE1   SLC10A3   SLC6A8   SLC9A6   SLITRK2   SLITRK4   SMIM10   SMIM9   SOX3   SPANXA1   SPANXA2   SPANXB1   SPANXC   SPANXD   SPANXN1   SPANXN2   SPANXN3   SPANXN4   SRPK3   SSR4   TAZ   TEX28   TKTL1   TMEM185A   TMEM187   TMLHE   TREX2   UBE2NL   UBL4A   VBP1   VGLL1   VMA21   ZFP92   ZIC3   ZNF185   ZNF275   ZNF449   ZNF75D  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X134,114,063 - 155,233,731CLINVAR
Cytogenetic MapXXq26.3-28CLINVAR

Additional Information

External Database Links
RGD Object Information
RGD ID: 12853565
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


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