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Items: 1 to 20 of 177

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131103insertion1nstd186human GRCh37 chr15: 65,282,232-65,282,254 , GRCh38.p12 chr15: 64,989,894-64,989,916 SPG21
    nsv5542308insertion1nstd206human GRCh38 chr15: 64,989,894-64,989,916 , GRCh37.p13 chr15: 65,282,232-65,282,254 SPG21
    nsv5516429copy number variation1nstd206human GRCh38 chr15: 64,971,228-64,972,637 , GRCh37.p13 chr15: 65,263,566-65,264,975 SPG21
    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
    nsv5308473copy number variation1nstd204human GRCh38.p13 chr15: 64,977,112-64,977,407 , GRCh37.p13 chr15: 65,269,450-65,269,745 SPG21
    nsv5155568mobile element insertion1nstd203human GRCh38 chr15: 64,975,465-64,975,465 , GRCh37.p13 chr15: 65,267,803-65,267,803 SPG21
    nsv4729728copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,221,723-65,365,642 , GRCh38.p12 chr15: 64,929,524-65,073,304 RASL12, SPG21, 4 more genes
    nsv4578100mobile element insertion1nstd166human GRCh37.p13 chr15: 65,278,322-65,278,322 , GRCh38.p12 chr15: 64,985,984-64,985,984 SPG21
    nsv4510489mobile element insertion1nstd166human GRCh37.p13 chr15: 65,261,000-65,261,000 , GRCh38.p12 chr15: 64,968,663-64,968,663 SPG21
    nsv4456887copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,258,583-65,742,148 , GRCh38.p12 chr15: 64,966,242-65,449,810 KBTBD13, SLC51B, 16 more genes
    nsv4456541copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,258,439-65,742,148 , GRCh38.p12 chr15: 64,966,098-65,449,810 CILP, SNORA24B, 16 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
    nsv4246121copy number variation1nstd166human GRCh37.p13 chr15: 65,276,343-65,276,564 , GRCh38.p12 chr15: 64,984,005-64,984,226 SPG21
    nsv4245633copy number variation1nstd166human GRCh37.p13 chr15: 65,263,642-65,264,893 , GRCh38.p12 chr15: 64,971,304-64,972,555 SPG21
    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
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
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