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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075791inversion1nstd229human GRCh38 chr15: 42,194,627-42,248,499 , GRCh37.p13 chr15: 42,486,825-42,540,697 TMEM87A, MIR627, 2 more genes
    nsv7062042inversion1nstd229human GRCh38 chr15: 38,786,391-46,534,887 , GRCh37.p13 chr15: 39,078,592-46,827,085 EHD4-AS1, PLA2G4B, 219 more genes
    nsv6973841copy number variation1nstd229human GRCh38 chr15: 41,876,434-43,470,213 , GRCh37.p13 chr15: 42,168,632-43,762,411 CAPN3, STARD9, 43 more genes
    nsv6973436copy number variation1nstd229human GRCh38 chr15: 42,255,367-42,259,614 , GRCh37.p13 chr15: 42,547,565-42,551,812 TMEM87A
    nsv6970347copy number variation1nstd229human GRCh38 chr15: 42,267,286-42,589,151 , GRCh37.p13 chr15: 42,559,484-42,881,349 LRRC57, GANC, 11 more genes
    nsv6964218copy number variation1nstd229human GRCh38 chr15: 41,758,370-42,299,821 , GRCh37.p13 chr15: 42,050,568-42,592,019 LOC105370793, RNA5SP393, 19 more genes
    nsv6959406copy number variation1nstd229human GRCh38 chr15: 42,248,603-42,391,378 , GRCh37.p13 chr15: 42,540,801-42,683,576 LOC105370794, GANC, 3 more genes
    nsv6593556inversion1nstd223human GRCh38 chr15: 42,262,763-42,263,451 , GRCh37.p13 chr15: 42,554,961-42,555,649 TMEM87A
    nsv6587307inversion1nstd223human GRCh38 chr15: 42,196,023-42,247,614 , GRCh37.p13 chr15: 42,488,221-42,539,812 VPS39, TMEM87A, 2 more genes
    nsv6583384inversion1nstd223human GRCh38 chr15: 42,238,367-42,239,146 , GRCh37.p13 chr15: 42,530,565-42,531,344 TMEM87A
    nsv6507073copy number variation1nstd223human GRCh38 chr15: 42,239,431-42,240,915 , GRCh37.p13 chr15: 42,531,629-42,533,113 TMEM87A
    nsv6132952copy number variation1nstd213human GRCh37 chr15: 42,480,000-43,110,001 , GRCh38.p12 chr15: 42,187,802-42,817,803 GANC, VPS39, 17 more genes
    nsv5707151mobile element insertion1nstd211human GRCh38 chr15: 42,227,188-42,227,188 , GRCh37.p13 chr15: 42,519,386-42,519,386 VPS39-DT, TMEM87A
    nsv5564072sequence alteration1nstd206human GRCh38 chr15: 42,194,628-42,248,498 , GRCh37.p13 chr15: 42,486,826-42,540,696 VPS39, TMEM87A, 2 more genes
    nsv5414817mobile element insertion1nstd206human GRCh38 chr15: 42,227,188-42,227,239 , GRCh37.p13 chr15: 42,519,386-42,519,437 VPS39-DT, TMEM87A
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5186220mobile element insertion1nstd203human GRCh38 chr15: 42,242,781-42,242,796 , GRCh37.p13 chr15: 42,534,979-42,534,994 TMEM87A
    nsv5158022mobile element insertion1nstd203human GRCh38 chr15: 42,242,781-42,242,796 , GRCh37.p13 chr15: 42,534,979-42,534,994 TMEM87A
    nsv5152162mobile element insertion1nstd203human GRCh38 chr15: 42,240,783-42,240,795 , GRCh37.p13 chr15: 42,532,981-42,532,993 TMEM87A
    nsv5151446mobile element insertion1nstd203human GRCh38 chr15: 42,246,659-42,246,678 , GRCh37.p13 chr15: 42,538,857-42,538,876 TMEM87A
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