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Variant : CV602633 (GRCh37/hg19 8q24.3(chr8:144379934-144399886)x1) Homo sapiens

Symbol: CV602633
Name: GRCh37/hg19 8q24.3(chr8:144379934-144399886)x1
Condition: not provided [RCV000747933]
Clinical Significance: benign
Last Evaluated: 10/25/2012
Review Status: no assertion criteria provided
Related Genes: TOP1MT   ZNF696  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh378144,379,934 - 144,399,886CLINVAR
Cytogenetic Map88q24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14363278
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-24
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.