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Variant : CV592426 (GRCh37/hg19 12p13.33(chr12:156857-186614)x1) Homo sapiens

Symbol: CV592426
Name: GRCh37/hg19 12p13.33(chr12:156857-186614)x1
Condition: not provided [RCV000737726]
Clinical Significance: benign
Last Evaluated: 05/25/2011
Review Status: no assertion criteria provided
Related Genes: IQSEC3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3712156,857 - 186,614CLINVAR
Cytogenetic Map1212p13.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353093
Created: 2019-02-12
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.