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Variant : CV381182 (GRCh37/hg19 15q24.2(chr15:75562397-75588048)x3) Homo sapiens

Symbol: CV381182
Name: GRCh37/hg19 15q24.2(chr15:75562397-75588048)x3
Condition: See cases [RCV000448009]
Clinical Significance: benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: GOLGA6C   GOLGA6D  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371575,562,397 - 75,588,048CLINVAR
Cytogenetic Map1515q24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852720
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-17
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.