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

Variant : CV593200 (GRCh37/hg19 14q23.1(chr14:58668869-58927173)x3) Homo sapiens

Symbol: CV593200
Name: GRCh37/hg19 14q23.1(chr14:58668869-58927173)x3
Condition: not provided [RCV000738500]
Clinical Significance: benign
Last Evaluated: 11/08/2012
Review Status: no assertion criteria provided
Related Genes: ACTR10   ARID4A   KIAA0586   PSMA3   TIMM9   TOMM20L  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371458,668,869 - 58,927,173CLINVAR
Cytogenetic Map1414q23.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14353880
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE


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