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Variant : CV437067 (GRCh37/hg19 3p24.2(chr3:25329791-25719030)x1) Homo sapiens

Symbol: CV437067
Name: GRCh37/hg19 3p24.2(chr3:25329791-25719030)x1
Condition: See cases [RCV000510441]
Clinical Significance: uncertain significance
Last Evaluated: 10/21/2014
Review Status: no assertion criteria provided
Related Genes: RARB   TOP2B  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37325,329,791 - 25,719,030CLINVAR
Cytogenetic Map33p24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13443420
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-05-19
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.