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Variant : CV594366 (GRCh37/hg19 17q25.1(chr17:72277879-72398544)x3) Homo sapiens

Symbol: CV594366
Name: GRCh37/hg19 17q25.1(chr17:72277879-72398544)x3
Condition: not provided [RCV000739666]
Clinical Significance: benign
Last Evaluated: 10/13/2014
Review Status: no assertion criteria provided
Related Genes: BTBD17   DNAI2   GPR142   KIF19  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371772,277,879 - 72,398,544CLINVAR
Cytogenetic Map1717q25.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14355040
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.