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Variant : CV599056 (GRCh37/hg19 5p15.33(chr5:1201599-1235790)x1) Homo sapiens

Symbol: CV599056
Name: GRCh37/hg19 5p15.33(chr5:1201599-1235790)x1
Condition: not provided [RCV000744356]
Clinical Significance: benign
Last Evaluated: 04/09/2014
Review Status: no assertion criteria provided
Related Genes: SLC6A18   SLC6A19  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3751,201,599 - 1,235,790CLINVAR
Cytogenetic Map55p15.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14359725
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.