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Variant : CV170929 (GRCh38/hg38 11p15.5(chr11:196966-244236)x1) Homo sapiens

Symbol: CV170929
Name: GRCh38/hg38 11p15.5(chr11:196966-244236)x1
Condition: See cases [RCV000050265]
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: BET1L   MIR6743   ODF3   PSMD13   RIC8A   SIRT3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_196966)_(244236_?)del
NC_000011.9:g.(?_196966)_(244236_?)del
NC_000011.8:g.(?_186966)_(234236_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3811196,966 - 244,236CLINVAR
GRCh3711196,966 - 244,236CLINVAR
Build 3611186,966 - 234,236CLINVAR
Cytogenetic Map1111p15.5CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9684520
Created: 2014-12-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.