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Variant : CV673347 (GRCh37/hg19 5p15.33(chr5:1088198-1274440)x3) Homo sapiens

Symbol: CV673347
Name: GRCh37/hg19 5p15.33(chr5:1088198-1274440)x3
Condition: not provided [RCV000846463]
Clinical Significance: uncertain significance
Last Evaluated: 05/04/2018
Review Status: no assertion criteria provided
Related Genes: SLC12A7   SLC6A18   SLC6A19   TERT  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3751,088,198 - 1,274,440CLINVAR
Cytogenetic Map55p15.33CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977028
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-20
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.