Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV158956 (GRCh38/hg38 10q26.3(chr10:132962729-133622588)x1) Homo sapiens

Symbol: CV158956
Name: GRCh38/hg38 10q26.3(chr10:132962729-133622588)x1
Condition: See cases [RCV000138257]
Clinical Significance: pathogenic|uncertain significance
Last Evaluated: 03/27/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ADAM8   ADGRA1   ADGRA1-AS1   CALY   CYP2E1   ECHS1   FUOM   KNDC1   LINC01166   LINC01168   MIR202   MIR202HG   MIR3944   MTG1   PAOX   PRAP1   SPRN   SYCE1   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_132962729)_(133622588_?)del
NC_000010.10:g.(?_134776233)_(135436092_?)del
NC_000010.9:g.(?_134626223)_(135286082_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3810132,962,729 - 133,622,588CLINVAR
GRCh3710134,776,233 - 135,436,092CLINVAR
Build 3610134,626,223 - 135,286,082CLINVAR
Cytogenetic Map1010q26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485806
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-01-07
Status: ACTIVE



NHLBI Logo

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