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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7063733inversion1nstd229human GRCh38 chr15: 63,479,684-65,571,065 , GRCh37.p13 chr15: 63,771,883-65,863,403 TRIP4, RNU5B-1, 45 more genes
    nsv6968329copy number variation1nstd229human GRCh38 chr15: 64,868,404-64,892,640 , GRCh37.p13 chr15: 65,160,603-65,184,839 PLEKHO2
    nsv6577595inversion1nstd223human GRCh38 chr15: 64,868,403-64,869,079 , GRCh37.p13 chr15: 65,160,602-65,161,278 PLEKHO2
    nsv6314072copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,978,681-65,679,053 , GRCh38.p12 chr15: 64,686,482-65,386,715 CLPX, RNU5B-1, 22 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv6093616insertion1nstd212human GRCh38 chr15: 64,843,580-64,843,580 , GRCh37.p13 chr15: 65,135,779-65,135,779 PLEKHO2
    nsv5664253insertion1nstd207human GRCh38 chr15: 64,843,579-64,843,579 , GRCh37.p13 chr15: 65,135,778-65,135,778 PLEKHO2
    nsv5525402copy number variation1nstd206human GRCh38 chr15: 64,868,317-64,869,351 , GRCh37.p13 chr15: 65,160,516-65,161,550 PLEKHO2
    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
    nsv5150184mobile element insertion1nstd203human GRCh38 chr15: 64,843,579-64,843,597 , GRCh37.p13 chr15: 65,135,778-65,135,796 PLEKHO2
    nsv5005504copy number variation1nstd200human GRCh38 chr15: 64,868,312-64,874,081 , GRCh37.p13 chr15: 65,160,511-65,166,280 PLEKHO2
    nsv4760118insertion1nstd199human GRCh37 chr15: 65,135,785-65,135,785 , GRCh38.p12 chr15: 64,843,586-64,843,586 PLEKHO2
    nsv4729193copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,705,736-65,178,188 , GRCh38.p12 chr15: 64,413,537-64,885,989 RBPMS2, GAPDHP61, 11 more genes
    nsv4626107copy number variation1nstd183human GRCh37 chr15: 65,135,758-65,249,721 , GRCh38.p12 chr15: 64,843,559-64,957,382 , PLEKHO2, 1 more genes
    nsv4384571copy number variation1nstd173human GRCh37 chr15: 65,096,792-65,258,596 , GRCh38.p12 chr15: 64,804,593-64,966,255 , ANKDD1A, 3 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
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