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Variant : CV592694 (GRCh37/hg19 12q21.33-22(chr12:91621655-96014946)x1) Homo sapiens

Symbol: CV592694
Name: GRCh37/hg19 12q21.33-22(chr12:91621655-96014946)x1
Condition: not provided [RCV000737994]
Clinical Significance: uncertain significance
Last Evaluated: 08/16/2011
Review Status: no assertion criteria provided
Related Genes: BTG1   CEP83   CLLU1   CLLU1-AS1   CRADD   EEA1   FGD6   LINC01619   METAP2   MIR492   MRPL42   NDUFA12   NR2C1   NUDT4   PLEKHG7   PLXNC1   SOCS2   TMCC3   UBE2N   USP44   VEZT  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371291,621,655 - 96,014,946CLINVAR
Cytogenetic Map1212q21.33-22CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353371
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-11
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.