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Variant : CV155348 (GRCh38/hg38 11p15.1(chr11:18526222-20748125)x3) Homo sapiens

Symbol: CV155348
Name: GRCh38/hg38 11p15.1(chr11:18526222-20748125)x3
Condition: See cases [RCV000134932]
Clinical Significance: uncertain significance
Last Evaluated: 01/14/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CSRP3   CSRP3-AS1   DBX1   E2F8   HTATIP2   IGSF22   LOC100126784   LOC110121487   LOC110121488   LOC111365162   LOC112067715   LOC112067716   MIR4486   MIR4694   MRGPRX1   MRGPRX2   NAV2   NAV2-AS2   NAV2-AS4   NAV2-AS5   NELL1   PRMT3   PTPN5   SLC6A5   SPTY2D1   SPTY2D1OS   TMEM86A   TSG101   UEVLD   ZDHHC13  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_18526222)_(20748125_?)dup
NC_000011.9:g.(?_18547769)_(20769671_?)dup
NC_000011.8:g.(?_18504345)_(20726247_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381118,526,222 - 20,748,125CLINVAR
GRCh371118,547,769 - 20,769,671CLINVAR
Build 361118,504,345 - 20,726,247CLINVAR
Cytogenetic Map1111p15.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482505
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.