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Variant : CV72201 (GRCh38/hg38 15q13.2-13.3(chr15:30438110-32607498)x3) Homo sapiens

Symbol: CV72201
Name: GRCh38/hg38 15q13.2-13.3(chr15:30438110-32607498)x3
Condition: Cognitive impairment [RCV000051339]|See cases [RCV000051339]
Clinical Significance: uncertain significance
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: ARHGAP11B   CHRNA7   FAN1   GOLGA8H   GOLGA8K   GOLGA8N   GOLGA8O   GOLGA8Q   KLF13   LINC02256   LINC02352   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.10:g.(?_30438110)_(32607498_?)dup
NC_000015.9:g.(?_30730313)_(32899699_?)dup
NC_000015.8:g.(?_28517605)_(30686991_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,438,110 - 32,607,498CLINVAR
GRCh371530,730,313 - 32,899,699CLINVAR
Build 361528,517,605 - 30,686,991CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8618360
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2019-10-15
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.