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Variant : CV673906 (GRCh37/hg19 2p25.1(chr2:11405245-12054698)x3) Homo sapiens

Symbol: CV673906
Name: GRCh37/hg19 2p25.1(chr2:11405245-12054698)x3
Condition: not provided [RCV000847022]
Clinical Significance: uncertain significance
Last Evaluated: 05/16/2018
Review Status: no assertion criteria provided
Related Genes: E2F6   GREB1   LINC00570   LPIN1   NTSR2   ROCK2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37211,405,245 - 12,054,698CLINVAR
Cytogenetic Map22p25.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977590
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-11-05
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.