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

Variant : CV435290 (GRCh37/hg19 12p13.33(chr12:173786-2108237)x3) Homo sapiens

Symbol: CV435290
Name: GRCh37/hg19 12p13.33(chr12:173786-2108237)x3
Condition: See cases [RCV000510561]
Clinical Significance: uncertain significance
Last Evaluated: 04/19/2015
Review Status: no assertion criteria provided
Related Genes: ADIPOR2   B4GALNT3   CACNA2D4   CCDC77   DCP1B   ERC1   FBXL14   IQSEC3   KDM5A   LRTM2   NINJ2   NINJ2-AS1   RAD52   SLC6A12   SLC6A13   WNK1   WNT5B  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3712173,786 - 2,108,237CLINVAR
Cytogenetic Map1212p13.33CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13443540
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-21
Status: ACTIVE


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