Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV555876 (GRCh37/hg19 Xp22.33-22.2(chrX:168546-16404364)x1) Homo sapiens

Symbol: CV555876
Name: GRCh37/hg19 Xp22.33-22.2(chrX:168546-16404364)x1
Condition: not provided [RCV000684181]
Clinical Significance: pathogenic
Last Evaluated: 10/30/2017
Review Status: no assertion criteria provided
Related Genes: ACE2   AMELX   ANOS1   AP1S2   ARHGAP6   ARSD   ARSD-AS1   ARSF   ARSH   ARSL   ASB11   ASB9   ATXN3L   BMX   CA5B   CLCN4   CLTRN   EGFL6   FAM9A   FAM9B   FAM9C   FANCB   FRMPD4   GEMIN8   GLRA2   GPM6B   GPR143   GRPR   GYG2   HCCS   INE2   MAGEB17   MID1   MOSPD2   MSL3   MXRA5   NLGN4X   OFD1   PIGA   PIR   PNPLA4   PRKX   PRPS2   PUDP   RAB9A   SHROOM2   STS   TBL1X   TCEANC   TLR7   TLR8   TMSB4X   TRAPPC2   VCX   VCX2   VCX3A   VCX3B   VEGFD   WWC3   XG   ZRSR2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X168,546 - 16,404,364CLINVAR
Cytogenetic MapXXp22.33-22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798281
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-01
Status: ACTIVE



NHLBI Logo

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