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Variant : CV383326 (GRCh37/hg19 12p13.33(chr12:173786-390463)x1) Homo sapiens

Symbol: CV383326
Name: GRCh37/hg19 12p13.33(chr12:173786-390463)x1
Condition: See cases [RCV000447695]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: IQSEC3   KDM5A   SLC6A12   SLC6A13  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712173,786 - 390,463CLINVAR
Cytogenetic Map1212p13.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12852409
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-07
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.