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Variant : CV159291 (GRCh38/hg38 Xp11.22(chrX:51701448-53065696)x0) Homo sapiens

Symbol: CV159291
Name: GRCh38/hg38 Xp11.22(chrX:51701448-53065696)x0
Condition: See cases [RCV000138538]
Clinical Significance: uncertain significance
Last Evaluated: 08/14/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CENPVL1   FAM156A   FAM156B   GPR173   GSPT2   MAGED1   MAGED4   MAGED4B   MIR8088   SNORA11D   SNORA11E   SPANXN5   SSX2   SSX2B   SSX7   XAGE1A   XAGE1B   XAGE2   XAGE3   XAGE5  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_51701448)_(53065696_?)del
NC_000023.10:g.(?_51436667)_(53047381_?)del
NC_000023.9:g.(?_51453407)_(53111603_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X51,701,448 - 53,065,696 (+)CLINVAR
GRCh37X51,436,667 - 53,047,381 (+)CLINVAR
Build 36X51,453,407 - 53,111,603CLINVAR
Cytogenetic MapXXp11.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486078
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.