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Variant : CV248309 (GRCh37/hg19 15q24.2(chr15:75562397-76030552)x3) Homo sapiens

Symbol: CV248309
Name: GRCh37/hg19 15q24.2(chr15:75562397-76030552)x3
Condition: See cases [RCV000240543]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: COMMD4   CSPG4   GOLGA6C   GOLGA6D   IMP3   MAN2C1   NEIL1   ODF3L1   PTPN9   SIN3A   SNUPN   SNX33  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371575,562,397 - 76,030,552CLINVAR
Cytogenetic Map1515q24.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541964
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2020-01-14
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.