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Variant : CV382147 (GRCh37/hg19 20p13(chr20:1427638-1638273)x3) Homo sapiens

Symbol: CV382147
Name: GRCh37/hg19 20p13(chr20:1427638-1638273)x3
Condition: See cases [RCV000448266]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: NSFL1C   SIRPB1   SIRPB2   SIRPD   SIRPG  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh37201,427,638 - 1,638,273CLINVAR
Cytogenetic Map2020p13CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 12852976
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.