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Variant : CV555882 (GRCh37/hg19 Xp22.33-22.12(chrX:201704-20682168)x3) Homo sapiens

Symbol: CV555882
Name: GRCh37/hg19 Xp22.33-22.12(chrX:201704-20682168)x3
Condition: not provided [RCV000684187]
Clinical Significance: pathogenic
Last Evaluated: 10/17/2017
Review Status: no assertion criteria provided
Related Genes: ACE2   ADGRG2   AMELX   ANOS1   AP1S2   ARHGAP6   ARSD   ARSD-AS1   ARSF   ARSH   ARSL   ASB11   ASB9   ATXN3L   BCLAF3   BEND2   BMX   CA5B   CDKL5   CLCN4   CLTRN   CTPS2   EGFL6   EIF1AX   FAM9A   FAM9B   FAM9C   FANCB   FRMPD4   GEMIN8   GLRA2   GPM6B   GPR143   GRPR   GYG2   HCCS   INE2   MAGEB17   MAP3K15   MAP7D2   MID1   MOSPD2   MSL3   MXRA5   NHS   NLGN4X   OFD1   PDHA1   PHKA2   PIGA   PIR   PNPLA4   PPEF1   PRKX   PRPS2   PUDP   RAB9A   RAI2   RBBP7   REPS2   RPS6KA3   RS1   S100G   SCML1   SCML2   SH3KBP1   SHROOM2   STS   SYAP1   TBL1X   TCEANC   TLR7   TLR8   TMSB4X   TRAPPC2   TXLNG   VCX   VCX2   VCX3A   VCX3B   VEGFD   WWC3   XG   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X201,704 - 20,682,168CLINVAR
Cytogenetic MapXXp22.33-22.12CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13798287
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE


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