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Variant : CV248463 (GRCh37/hg19 15q24.1-24.3(chr15:74368270-78122737)x3) Homo sapiens

Symbol: CV248463
Name: GRCh37/hg19 15q24.1-24.3(chr15:74368270-78122737)x3
Condition: See cases [RCV000240526]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ARID3B   C15orf39   CCDC33   CLK3   COMMD4   COX5A   CPLX3   CSK   CSPG4   CYP11A1   CYP1A1   CYP1A2   EDC3   ETFA   FAM219B   FBXO22   GOLGA6A   GOLGA6C   GOLGA6D   HMG20A   IMP3   ISL2   ISLR   ISLR2   LINGO1   LMAN1L   MAN2C1   MPI   NEIL1   NRG4   ODF3L1   PEAK1   PPCDC   PSTPIP1   PTPN9   RCN2   RPP25   SCAMP2   SCAMP5   SCAPER   SEMA7A   SIN3A   SNUPN   SNX33   STRA6   TMEM266   TSPAN3   UBE2Q2   UBL7   ULK3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_74368270)_(78122737_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371574,368,270 - 78,122,737CLINVAR
Cytogenetic Map1515q24.1-24.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 11541910
Created: 2016-10-11
Species: Homo sapiens
Last Modified: 2019-08-06
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.