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Variant : CV164927 (GRCh38/hg38 7q35(chr7:143733925-144255312)x3) Homo sapiens

Symbol: CV164927
Name: GRCh38/hg38 7q35(chr7:143733925-144255312)x3
Condition: See cases [RCV000143240]
Clinical Significance: uncertain significance
Last Evaluated: 12/10/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGEF35   ARHGEF35-AS1   CTAGE4   CTAGE6   OR2A1-AS1   OR2A12   OR2A14   OR2A2   OR2A25   OR2A42   OR2A5   OR2F1   OR2F2   OR6B1   TCAF1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_143733925)_(144255312_?)dup
NC_000007.13:g.(?_143431018)_(143952405_?)dup
NC_000007.12:g.(?_143061951)_(143583338_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh387143,733,925 - 144,255,312CLINVAR
GRCh377143,431,018 - 143,952,405CLINVAR
Build 367143,061,951 - 143,583,338CLINVAR
Cytogenetic Map77q35CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490838
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.