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Variant : CV156461 (GRCh38/hg38 10q25.2-25.3(chr10:112074094-115537174)x1) Homo sapiens

Symbol: CV156461
Name: GRCh38/hg38 10q25.2-25.3(chr10:112074094-115537174)x1
Condition: See cases [RCV000135960]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2009
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABLIM1   ACSL5   ADRB1   AFAP1L2   ATRNL1   CASP7   CCDC186   DCLRE1A   FAM160B1   GPAM   HABP2   LINC02626   MIR2110   MIR4295   MIR4483   MIR6715A   MIR6715B   NHLRC2   NRAP   PLEKHS1   SNORA87   TCF7L2   TDRD1   TECTB   TRUB1   VTI1A   VWA2   ZDHHC6  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_112074094)_(115537174_?)del
NC_000010.10:g.(?_113833852)_(117032437_?)del
NC_000010.9:g.(?_113823842)_(117286674_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810112,074,094 - 115,537,174CLINVAR
GRCh3710113,833,852 - 117,032,437 (+)CLINVAR
Build 3610113,823,842 - 117,286,674CLINVAR
Cytogenetic Map1010q25.2-25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9483526
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-07-09
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.