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Variant : CV606934 (GRCh37/hg19 17q25.3(chr17:79857137-79986312)x3) Homo sapiens

Symbol: CV606934
Name: GRCh37/hg19 17q25.3(chr17:79857137-79986312)x3
Condition: not provided [RCV000752234]
Clinical Significance: benign
Last Evaluated: 03/15/2013
Review Status: no assertion criteria provided
Related Genes: ANAPC11   ASPSCR1   CENPX   LRRC45   MAFG   MYADML2   NOTUM   NPB   PCYT2   PYCR1   SIRT7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371779,857,137 - 79,986,312CLINVAR
Cytogenetic Map1717q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14367558
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.