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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6966760copy number variation1nstd229human GRCh38 chr15: 80,835,041-80,847,644 , GRCh37.p13 chr15: 81,127,382-81,139,985 CEMIP, MIR549A
    nsv6513606copy number variation1nstd223human GRCh38 chr15: 80,838,108-80,840,213 , GRCh37.p13 chr15: 81,130,449-81,132,554 CEMIP, MIR549A
    nsv5001972copy number variation1nstd200human GRCh38 chr15: 80,838,171-80,840,240 , GRCh37.p13 chr15: 81,130,512-81,132,581 MIR549A, CEMIP
    nsv4856040copy number variation1nstd200human GRCh37 chr15: 81,130,526-81,132,554 , GRCh38.p12 chr15: 80,838,185-80,840,213 MIR549A, CEMIP
    nsv5009097copy number variation1nstd200human GRCh38 chr15: 80,837,834-80,840,591 , GRCh37.p13 chr15: 81,130,175-81,132,932 MIR549A, CEMIP
    nsv7062305inversion1nstd229human GRCh38 chr15: 80,841,070-80,844,442 , GRCh37.p13 chr15: 81,133,411-81,136,783 MIR549A, CEMIP
    nsv6965791copy number variation1nstd229human GRCh38 chr15: 80,776,401-80,977,900 , GRCh37.p13 chr15: 81,068,742-81,270,241 CEMIP, MIR549A, 1 more genes
    nsv1194780copy number variation1nstd113human NCBI36 chr15: 78,843,467-78,975,902 , GRCh37.p13 chr15: 81,056,412-81,188,847 , GRCh38.p12 chr15: 80,764,071-80,896,506 MIR549A, CEMIP, 1 more genes
    esv3789695tandem duplication1estd192human GRCh37 chr15: 81,052,426-81,190,178 , GRCh38.p12 chr15: 80,760,085-80,897,837 MIR549A, CEMIP, 1 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
    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
    nsv4456639copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,728,654-84,107,646 , GRCh38.p12 chr15: 80,436,313-83,438,894 LOC100288241, LOC105370926, 64 more genes
    nsv3905472copy number variation1nstd102humanPathogenic GRCh37 chr15: 80,703,867-83,955,596 , GRCh38.p12 chr15: 80,411,525-83,286,844 LINC01583, MIR5572, 62 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 MYZAP, JMJD7, 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 MIR4513, LOC727751, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 TMEM202, SNORD115-28, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 FES, OR4H6BP, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 FAM81A, LOC105370884, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 RNU6-953P, LOC105370805, 1385 more genes
    nsv3899559copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595 CILP, HDDC3, 1176 more genes
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