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Variant : CV162577 (GRCh38/hg38 11p11.2(chr11:46420955-46728372)x3) Homo sapiens

Symbol: CV162577
Name: GRCh38/hg38 11p11.2(chr11:46420955-46728372)x3
Condition: See cases [RCV000141333]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMBRA1   ARHGAP1   ATG13   F2   HARBI1   MIR3160-1   MIR3160-2   ZNF408  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_46420955)_(46728372_?)dup
NC_000011.9:g.(?_46442505)_(46749922_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381146,420,955 - 46,728,372CLINVAR
GRCh371146,442,505 - 46,749,922CLINVAR
Build 361146,399,081 - 46,706,498CLINVAR
Cytogenetic Map1111p11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488858
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.