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Variant : CV382104 (GRCh37/hg19 12p13.33(chr12:91682-176816)x3) Homo sapiens

Symbol: CV382104
Name: GRCh37/hg19 12p13.33(chr12:91682-176816)x3
Condition: See cases [RCV000448159]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: IQSEC3  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371291,682 - 176,816CLINVAR
Cytogenetic Map1212p13.33CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 12852869
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-14
Status: ACTIVE


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