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Variant : CV165042 (GRCh38/hg38 6q26(chr6:160892889-161535434)x3) Homo sapiens

Symbol: CV165042
Name: GRCh38/hg38 6q26(chr6:160892889-161535434)x3
Condition: See cases [RCV000143355]
Clinical Significance: uncertain significance
Last Evaluated: 04/16/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AGPAT4   AGPAT4-IT1   MAP3K4   PRKN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_160892889)_(161535434_?)dup
NC_000006.11:g.(?_161313921)_(161956466_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh386160,892,889 - 161,535,434CLINVAR
GRCh376161,313,921 - 161,956,466CLINVAR
Build 366161,233,911 - 161,876,456CLINVAR
Cytogenetic Map66q26CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9490953
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-12-03
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.