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Variant : CV613288 (GRCh37/hg19 15q24.1(chr15:73436105-73502838)x1) Homo sapiens

Symbol: CV613288
Name: GRCh37/hg19 15q24.1(chr15:73436105-73502838)x1
Condition: not provided [RCV000762694]
Clinical Significance: likely benign
Last Evaluated: 04/10/2018
Review Status: criteria provided, single submitter
Related Genes: NEO1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371573,436,105 - 73,502,838CLINVAR
Cytogenetic Map1515q24.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14397448
Created: 2019-04-09
Species: Homo sapiens
Last Modified: 2019-06-18
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.