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Variant : CV160522 (GRCh38/hg38 Xp11.22(chrX:51521752-52274330)x0) Homo sapiens

Symbol: CV160522
Name: GRCh38/hg38 Xp11.22(chrX:51521752-52274330)x0
Condition: See cases [RCV000139583]
Clinical Significance: uncertain significance
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CENPVL1   CENPVL2   CENPVL3   GSPT2   MAGED1   MAGED4   MAGED4B   SNORA11D   SNORA11E  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_51521752)_(52274330_?)del
NC_000023.9:g.(?_51281344)_(52034197_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X51,521,752 - 52,274,330CLINVAR
Build 36X51,281,344 - 52,034,197CLINVAR
Cytogenetic MapXXp11.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487114
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-10
Status: ACTIVE



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