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Variant : CV158972 (GRCh38/hg38 7q35(chr7:143560424-144169056)x3) Homo sapiens

Symbol: CV158972
Name: GRCh38/hg38 7q35(chr7:143560424-144169056)x3
Condition: See cases [RCV000138272]
Clinical Significance: likely benign
Last Evaluated: 06/01/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CTAGE15   CTAGE6   OR2A12   OR2A14   OR2A2   OR2A25   OR2A5   OR2F1   OR2F2   OR6B1   TCAF1   TCAF2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000007.14:g.(?_143560424)_(144169056_?)dup
NC_000007.13:g.(?_143257517)_(143866149_?)dup
NC_000007.12:g.(?_142967639)_(143497082_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh387143,560,424 - 144,169,056CLINVAR
GRCh377143,257,517 - 143,866,149CLINVAR
Build 367142,967,639 - 143,497,082CLINVAR
Cytogenetic Map77q35CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9485821
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-04
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.