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Variant : CV158534 (GRCh38/hg38 11p15.1-14.2(chr11:21838014-26738627)x3) Homo sapiens

Symbol: CV158534
Name: GRCh38/hg38 11p15.1-14.2(chr11:21838014-26738627)x3
Condition: See cases [RCV000137849]
Clinical Significance: uncertain significance
Last Evaluated: 10/10/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ANO3   ANO3-AS1   ANO5   CCDC179   FANCF   GAS2   LINC01495   LINC02686   LINC02699   LINC02718   LINC02726   LOC113939921   LUZP2   MIR8054   MUC15   SLC17A6   SLC5A12   SVIP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_21838014)_(26738627_?)dup
NC_000011.9:g.(?_21859560)_(26760174_?)dup
NC_000011.8:g.(?_21816136)_(26716750_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381121,838,014 - 26,738,627CLINVAR
GRCh371121,859,560 - 26,760,174CLINVAR
Build 361121,816,136 - 26,716,750CLINVAR
Cytogenetic Map1111p15.1-14.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485401
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.