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Variant : CV156540 (GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1) Homo sapiens

Symbol: CV156540
Name: GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1
Condition: See cases [RCV000136028]
Clinical Significance: pathogenic
Last Evaluated: 10/30/2010
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   EEF1AKMT2   FAM53B   FAM53B-AS1   FANK1   FANK1-AS1   FOXI2   FUOM   GLRX3   INPP5A   INSYN2A   JAKMIP3   KNDC1   LHPP   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)
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_124473108)_(133620609_?)del
Human AssemblyChrPosition (strand)Source
GRCh3810124,473,108 - 133,620,609CLINVAR
GRCh3710126,161,677 - 135,434,113CLINVAR
Build 3610126,151,667 - 135,284,103CLINVAR
Cytogenetic Map1010q26.13-26.3CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 9483591
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.