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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071130inversion1nstd229human GRCh38 chr15: 33,339,608-35,270,089 , GRCh37.p13 chr15: 33,631,809-35,562,290 LOC105370765, AQR, 38 more genes
    nsv7067070inversion1nstd229human GRCh38 chr15: 32,727,797-34,288,910 , GRCh37.p13 chr15: 33,019,998-34,581,111 HNRNPA1P71, FMN1, 16 more genes
    nsv7063469inversion1nstd229human GRCh38 chr15: 33,686,568-35,388,285 , GRCh37.p13 chr15: 33,978,769-35,680,486 NUTM1, AVEN, 41 more genes
    nsv6972984copy number variation1nstd229human GRCh38 chr15: 34,105,673-34,106,998 , GRCh37.p13 chr15: 34,397,874-34,399,199 PGBD4
    nsv6969948copy number variation1nstd229human GRCh38 chr15: 32,139,827-34,373,967 , GRCh37.p13 chr15: 32,432,028-34,666,168 AVEN, LPCAT4, 50 more genes
    nsv6968810copy number variation1nstd229human GRCh38 chr15: 34,060,646-34,221,642 , GRCh37.p13 chr15: 34,352,847-34,513,843 AVEN, RPL32P2, 4 more genes
    nsv6962698copy number variation1nstd229human GRCh38 chr15: 33,805,701-34,143,000 , GRCh37.p13 chr15: 34,097,902-34,435,201 CHRM5, EMC7, 5 more genes
    nsv6637455copy number variation1nstd102humanUncertain significance GRCh37 chr15: 33,785,125-34,488,132 , GRCh38.p12 chr15: 33,492,924-34,195,931 EMC7, RPL32P2, 6 more genes
    nsv6634442copy number variation1nstd102humanPathogenic GRCh37 chr15: 32,915,722-34,671,601 , GRCh38.p12 chr15: 32,623,521-34,379,400 KATNBL1, ARHGAP11A, 27 more genes
    nsv6595043inversion1nstd223human GRCh38 chr15: 34,106,939-34,137,253 , GRCh37.p13 chr15: 34,399,140-34,429,454 PGBD4
    nsv6578421inversion1nstd223human GRCh38 chr15: 34,099,702-34,100,201 , GRCh37.p13 chr15: 34,391,903-34,392,402 PGBD4, EMC7
    nsv6515036copy number variation1nstd223human GRCh38 chr15: 34,094,429-34,106,369 , GRCh37.p13 chr15: 34,386,630-34,398,570 EMC7, PGBD4
    nsv6514134copy number variation1nstd223human GRCh38 chr15: 34,104,524-34,106,306 , GRCh37.p13 chr15: 34,396,725-34,398,507 PGBD4
    nsv6504513copy number variation1nstd223human GRCh38 chr15: 34,107,823-34,112,177 , GRCh37.p13 chr15: 34,400,024-34,404,378 PGBD4
    nsv6502869copy number variation1nstd223human GRCh38 chr15: 33,970,001-34,711,900 , GRCh37.p13 chr15: 34,262,202-35,004,101 LINC02252, GOLGA8A, 20 more genes
    nsv6497505copy number variation1nstd223human GRCh38 chr15: 32,139,826-34,373,966 , GRCh37.p13 chr15: 32,432,027-34,666,167 TMCO5B, LPCAT4, 50 more genes
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6241894mobile element insertion1nstd215human GRCh38 chr15: 34,105,884-34,105,884 , GRCh37.p13 chr15: 34,398,085-34,398,085 PGBD4
    nsv6132891copy number variation1nstd213human GRCh37 chr15: 34,380,000-34,660,001 , GRCh38.p12 chr15: 34,087,799-34,367,800 SLC12A6, EMC4, 6 more genes
    nsv6032809copy number variation1nstd212human GRCh38 chr15: 34,107,952-34,138,754 , GRCh37.p13 chr15: 34,400,153-34,430,955 KATNBL1, PGBD4
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