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Variant : CV555379 (GRCh37/hg19 15q15.1(chr15:42079854-42426833)x3) Homo sapiens

Symbol: CV555379
Name: GRCh37/hg19 15q15.1(chr15:42079854-42426833)x3
Condition: not provided [RCV000683684]
Clinical Significance: uncertain significance
Last Evaluated: 12/15/2017
Review Status: no assertion criteria provided
Related Genes: EHD4   JMJD7   MAPKBP1   PLA2G4B   PLA2G4D   PLA2G4E   SPTBN5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371542,079,854 - 42,426,833CLINVAR
Cytogenetic Map1515q15.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13797360
Created: 2018-10-09
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.