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Variant : CV382428 (GRCh37/hg19 8q13.3(chr8:71549662-71647145)x3) Homo sapiens

Symbol: CV382428
Name: GRCh37/hg19 8q13.3(chr8:71549662-71647145)x3
Condition: See cases [RCV000448894]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: LACTB2   XKR9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37871,549,662 - 71,647,145CLINVAR
Cytogenetic Map88q13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853594
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.