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Variant : CV614053 (GRCh37/hg19 15q24.2(chr15:75648132-76102251)) Homo sapiens

Symbol: CV614053
Name: GRCh37/hg19 15q24.2(chr15:75648132-76102251)
Condition: not provided [RCV000767757]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: CSPG4   IMP3   MAN2C1   ODF3L1   PTPN9   SIN3A   SNUPN   SNX33  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371575,648,132 - 76,102,251CLINVAR
Cytogenetic Map1515q24.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14399710
Created: 2019-05-07
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.