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Variant : CV673351 (GRCh37/hg19 15q24.2(chr15:75309345-75930806)x3) Homo sapiens

Symbol: CV673351
Name: GRCh37/hg19 15q24.2(chr15:75309345-75930806)x3
Condition: not provided [RCV000846467]
Clinical Significance: uncertain significance
Last Evaluated: 05/10/2018
Review Status: no assertion criteria provided
Related Genes: C15orf39   COMMD4   GOLGA6C   GOLGA6D   MAN2C1   NEIL1   PPCDC   PTPN9   SCAMP5   SIN3A   SNUPN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371575,309,345 - 75,930,806CLINVAR
Cytogenetic Map1515q24.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14977032
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-31
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.