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Variant : CV158394 (GRCh38/hg38 Xq27.3(chrX:145295181-146025530)x3) Homo sapiens

Symbol: CV158394
Name: GRCh38/hg38 Xq27.3(chrX:145295181-146025530)x3
Condition: See cases [RCV000137711]
Clinical Significance: likely benign
Last Evaluated: 12/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR888   MIR890   MIR891B   MIR892A   MIR892B   MIR892C   SLITRK2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_145295181)_(146025530_?)dup
NW_004070890.2:g.(?_819574)_(1549921_?)dup
NC_000023.9:g.(?_144184393)_(144914740_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X145,295,181 - 146,025,530CLINVAR
Build 36X144,184,393 - 144,914,740CLINVAR
Cytogenetic MapXXq27.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485263
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.