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Variant : CV599037 (GRCh37/hg19 5p15.33(chr5:403286-685504)x3) Homo sapiens

Symbol: CV599037
Name: GRCh37/hg19 5p15.33(chr5:403286-685504)x3
Condition: not provided [RCV000744337]
Clinical Significance: benign
Last Evaluated: 09/14/2011
Review Status: no assertion criteria provided
Related Genes: AHRR   CEP72   EXOC3   EXOC3-AS1   SLC9A3   TPPP  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh375403,286 - 685,504CLINVAR
Cytogenetic Map55p15.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14359706
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.