U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 30

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674850copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,011,048-49,137,179 , GRCh38.p12 chr15: 48,718,851-48,844,982 SHC4, LOC645405, 1 more genes
    nsv4455809copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,043,112-49,286,126 , GRCh38.p12 chr15: 48,750,915-48,993,929 SHC4, KRT8P24, 3 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 SHC4, H3P40, 1616 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 SHC4, RNU6-18P, 1442 more genes
    nsv3903255copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,689,327-52,446,981 , GRCh38.p12 chr15: 41,397,129-52,154,784 SHC4, RN7SKP101, 234 more genes
    nsv3903669copy number variation1nstd102humanPathogenic GRCh37 chr15: 43,759,773-53,252,240 , GRCh38.p12 chr15: 43,467,575-52,960,043 SHC4, MIR4712, 188 more genes
    nsv6313917copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,635,238-56,509,908 , GRCh38.p12 chr15: 47,343,041-56,217,710 SHC4, PYGO1, 125 more genes
    nsv3902367copy number variation1nstd102humanPathogenic GRCh37 chr15: 42,850,434-49,592,633 , GRCh38.p12 chr15: 42,558,236-49,300,436 SHC4, SERF2-C15ORF63, 142 more genes
    nsv4769387copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,744,917-53,851,050 , GRCh38.p12 chr15: 48,452,720-53,558,853 SHC4, BCL2L10, 86 more genes
    nsv3917643copy number variation1nstd102humanPathogenic GRCh38 chr15: 47,460,844-52,494,222 , GRCh37 chr15: 47,753,041-52,786,419 , NCBI36 chr15: 45,540,333-50,573,711 SHC4, LOC105370819, 86 more genes
    nsv4675095copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,192,561-50,819,726 , GRCh38.p12 chr15: 46,900,363-50,527,529 SHC4, LOC102724587, 51 more genes
    nsv3906553copy number variation1nstd102humanPathogenic GRCh37 chr15: 47,574,384-50,369,056 , GRCh38.p12 chr15: 47,282,187-50,076,859 SHC4, LOC105370811, 36 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 SHC4, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 SHC4, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 SHC4, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 SHC4, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 SHC4, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 SHC4, RNU6-953P, 1385 more genes
    nsv3899559copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595 SHC4, CILP, 1176 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 SHC4, LINC03065, 228 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center