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Variant : CV535447 (NC_000015.10:g.(?_74071509)_(77878298_?)dup) Homo sapiens

Symbol: CV535447
Name: NC_000015.10:g.(?_74071509)_(77878298_?)dup
Condition: Schizophrenia [RCV000754167]
Clinical Significance: likely pathogenic
Last Evaluated: 03/20/2018
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   LINC00597   LINC02255   LINGO1   LINGO1-AS1   LINGO1-AS2   LMAN1L   MAN2C1   MIR3713   MIR4313   MIR4513   MIR631   MIR6881   MIR6882   MPI   NEIL1   NRG4   ODF3L1   PEAK1   PPCDC   PSTPIP1   PTPN9   RCN2   RPP25   SCAMP2   SCAMP5   SCAPER   SEMA7A   SIN3A   SNUPN   SNX33   STRA6   TMEM266   TSPAN3   UBE2Q2   UBL7   UBL7-AS1   ULK3  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: research
HGVS Name(s): NC_000015.10:g.(?_74071509)_(77878298_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381574,071,509 - 77,878,298CLINVAR
Cytogenetic Map1515q24.1-24.3CLINVAR
Trait Synonyms: SCHIZOPHRENIA WITH OR WITHOUT AN AFFECTIVE DISORDER



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352162
Created: 2019-02-12
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.