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

Variant : CV555972 (GRCh37/hg19 Xp22.2(chrX:15486059-16018163)x3) Homo sapiens

Symbol: CV555972
Name: GRCh37/hg19 Xp22.2(chrX:15486059-16018163)x3
Condition: not provided [RCV000684277]
Clinical Significance: uncertain significance
Last Evaluated: 04/16/2018
Review Status: no assertion criteria provided
Related Genes: ACE2   AP1S2   BMX   CA5B   CLTRN   INE2   PIR   ZRSR2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37X15,486,059 - 16,018,163CLINVAR
Cytogenetic MapXXp22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798390
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-10-08
Status: ACTIVE



NHLBI Logo

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