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

Variant : CV435584 (GRCh37/hg19 Xq28(chrX:152899437-153624564)x2) Homo sapiens

Symbol: CV435584
Name: GRCh37/hg19 Xq28(chrX:152899437-153624564)x2
Condition: See cases [RCV000512403]
Clinical Significance: pathogenic
Last Evaluated: 04/22/2014
Review Status: no assertion criteria provided
Related Genes: ABCD1   ARHGAP4   AVPR2   BCAP31   DUSP9   EMD   FLNA   HCFC1   IDH3G   IRAK1   L1CAM   MECP2   NAA10   OPN1LW   OPN1MW   OPN1MW2   PDZD4   PLXNB3   PNCK   RENBP   SLC6A8   SRPK3   SSR4   TEX28   TKTL1   TMEM187  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37X152,899,437 - 153,624,564CLINVAR
Cytogenetic MapXXq28CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13445365
Created: 2017-11-07
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.