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Variant : CV160527 (GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1) Homo sapiens

Symbol: CV160527
Name: GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1
Condition: See cases [RCV000139588]
Clinical Significance: pathogenic
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: 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  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_125021995)_(133620609_?)del
NC_000010.10:g.(?_126710564)_(135434113_?)del
NC_000010.9:g.(?_126700554)_(135284103_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810125,021,995 - 133,620,609CLINVAR
GRCh3710126,710,564 - 135,434,113CLINVAR
Build 3610126,700,554 - 135,284,103CLINVAR
Cytogenetic Map1010q26.13-26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487119
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-14
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.