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Variant : CV160725 (GRCh38/hg38 7q35(chr7:143735880-144155736)x3) Homo sapiens

Symbol: CV160725
Name: GRCh38/hg38 7q35(chr7:143735880-144155736)x3
Condition: See cases [RCV000139760]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CTAGE6   OR2A12   OR2A14   OR2A2   OR2A25   OR2A5   OR2F1   OR2F2   OR6B1   TCAF1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_143735880)_(144155736_?)dup
NC_000007.13:g.(?_143432973)_(143852829_?)dup
NC_000007.12:g.(?_143063906)_(143483762_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh387143,735,880 - 144,155,736CLINVAR
GRCh377143,432,973 - 143,852,829CLINVAR
Build 367143,063,906 - 143,483,762CLINVAR
Cytogenetic Map77q35CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487290
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.