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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 LOC105370892, MRPS15P1, 99 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094304copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,978,569-75,190,071 , GRCh38.p12 chr15: 72,686,228-74,897,730 TBC1D21, LOC105370893, 60 more genes
    nsv7077484inversion1nstd229human GRCh38 chr15: 74,072,224-75,785,570 , GRCh37.p13 chr15: 74,364,565-76,077,911 LOC107984720, SCAMP2, 68 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7066327inversion1nstd229human GRCh38 chr15: 74,062,424-75,303,012 , GRCh37.p13 chr15: 74,354,765-75,595,353 FAM219B, PPCDC, 48 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6971274copy number variation1nstd229human GRCh38 chr15: 74,665,201-74,824,500 , GRCh37.p13 chr15: 74,957,542-75,116,841 CSK, CYP1A1, 4 more genes
    nsv6968427copy number variation1nstd229human GRCh38 chr15: 74,723,443-74,758,388 , GRCh37.p13 chr15: 75,015,784-75,050,729 CYP1A1, CYP1A2
    nsv6959949copy number variation1nstd229human GRCh38 chr15: 74,747,021-74,774,648 , GRCh37.p13 chr15: 75,039,362-75,066,989 CYP1A2
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 PTPN9, NRG4, 96 more genes
    nsv6595490inversion1nstd223human GRCh38 chr15: 74,067,732-75,273,464 , GRCh37.p13 chr15: 74,360,073-75,565,805 CCDC33, LOC107984772, 44 more genes
    nsv6594805inversion1nstd223human GRCh38 chr15: 74,067,653-75,273,541 , GRCh37.p13 chr15: 74,359,994-75,565,882 PPCDC, COMMD4P2, 44 more genes
    nsv6592543inversion1nstd223human GRCh38 chr15: 74,064,999-75,300,334 , GRCh37.p13 chr15: 74,357,340-75,592,675 GOLGA6A, MIR6882, 48 more genes
    nsv6581686inversion1nstd223human GRCh38 chr15: 74,747,271-74,747,869 , GRCh37.p13 chr15: 75,039,612-75,040,210 CYP1A2
    nsv6315505copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,398,068-76,054,094 , GRCh38.p12 chr15: 74,105,727-75,761,753 RPL36AP45, GOLGA6D, 62 more genes
    nsv6309590copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,978,569-75,722,716 , GRCh38.p12 chr15: 72,686,228-75,430,375 NPM1P42, MAN2C1, 82 more genes
    nsv6291818copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,047,425-75,073,422 , GRCh38.p12 chr15: 74,755,084-74,781,081 CSK, CYP1A2
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