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Variant : CV674035 (GRCh37/hg19 17q25.3(chr17:76857398-77308782)x3) Homo sapiens

Symbol: CV674035
Name: GRCh37/hg19 17q25.3(chr17:76857398-77308782)x3
Condition: not provided [RCV000847151]
Clinical Significance: uncertain significance
Last Evaluated: 12/28/2017
Review Status: no assertion criteria provided
Related Genes: C1QTNF1   CANT1   ENGASE   LGALS3BP   RBFOX3   TIMP2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371776,857,398 - 77,308,782CLINVAR
Cytogenetic Map1717q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977732
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.