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Variant : CV162798 (GRCh38/hg38 6q21(chr6:110020558-111200711)x3) Homo sapiens

Symbol: CV162798
Name: GRCh38/hg38 6q21(chr6:110020558-111200711)x3
Condition: See cases [RCV000141546]
Clinical Significance: uncertain significance
Last Evaluated: 09/16/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMD1   CDC40   CDK19   DDO   GTF3C6   METTL24   RPF2   SLC16A10   SLC22A16   SNORA40C   SNORD166   WASF1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000006.12:g.(?_110020558)_(111200711_?)dup
NC_000006.11:g.(?_110341761)_(111521914_?)dup
NC_000006.10:g.(?_110448454)_(111628607_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh386110,020,558 - 111,200,711CLINVAR
GRCh376110,341,761 - 111,521,914CLINVAR
Build 366110,448,454 - 111,628,607CLINVAR
Cytogenetic Map66q21CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489071
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.