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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   AL137025.1   AL158212.3   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
 
CRRD Object Information
CRRD ID: 9483526
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-07-28
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.