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Variant : CV160751 (GRCh38/hg38 10q25.2-25.3(chr10:110804735-114884010)x1) Homo sapiens

Symbol: CV160751
Name: GRCh38/hg38 10q25.2-25.3(chr10:110804735-114884010)x1
Condition: See cases [RCV000139783]
Clinical Significance: likely pathogenic
Last Evaluated: 10/24/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABLIM1   ACSL5   ADRA2A   ADRB1   AFAP1L2   AL137025.1   AL158212.3   BBIP1   CASP7   CCDC186   DCLRE1A   FAM160B1   FRA10B   GPAM   HABP2   MIR2110   MIR4295   MIR4483   MIR4680   MIR548E   MIR6715A   MIR6715B   NHLRC2   NRAP   PDCD4   PDCD4-AS1   PLEKHS1   RBM20   SHOC2   SNORA87   TCF7L2   TDRD1   TECTB   VTI1A   VWA2   ZDHHC6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_110804735)_(114884010_?)del
NC_000010.10:g.(?_112564493)_(116643769_?)del
NC_000010.9:g.(?_112554483)_(116633759_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810110,804,735 - 114,884,010CLINVAR
GRCh3710112,564,493 - 116,643,769CLINVAR
Build 3610112,554,483 - 116,633,759CLINVAR
Cytogenetic Map1010q25.2-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487313
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.