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Variant : CV158331 (GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1) Homo sapiens

Symbol: CV158331
Name: GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1
Condition: See cases [RCV000137653]
Clinical Significance: pathogenic
Last Evaluated: 09/12/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABRAXAS2   ADAM12   ADAM8   ADGRA1   ADGRA1-AS1   BCCIP   BNIP3   C10orf143   C10orf90   CALY   CFAP46   CLRN3   CTBP2   CYP2E1   DHX32   DOCK1   DPYSL4   EBF3   ECHS1   EDRF1   EDRF1-AS1   EDRF1-DT   FANK1   FANK1-AS1   FOXI2   FUOM   GLRX3   INPP5A   INSYN2A   JAKMIP3   KNDC1   LINC00601   LINC01163   LINC01164   LINC01165   LINC01166   LINC01167   LINC01168   LINC02667   LINC02870   LRRC27   MGMT   MIR202   MIR202HG   MIR378C   MIR3944   MIR4296   MIR4297   MIR4484   MKI67   MMP21   MTG1   NKX6-2   NPS   PAOX   PPP2R2D   PRAP1   PTPRE   PWWP2B   SPRN   STK32C   SYCE1   TCERG1L   TCERG1L-AS1   TEX36   TEX36-AS1   TUBGCP2   UROS   UTF1   VENTX   ZNF511   ZRANB1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_124834858)_(133622588_?)del
NC_000010.10:g.(?_126523427)_(135436092_?)del
NC_000010.9:g.(?_126513417)_(135286082_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810124,834,858 - 133,622,588CLINVAR
GRCh3710126,523,427 - 135,436,092CLINVAR
Build 3610126,513,417 - 135,286,082CLINVAR
Cytogenetic Map1010q26.13-26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485206
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
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.