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Items: 1 to 20 of 344

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6307928insertion1nstd186human GRCh37 chr3: 111,856,438-111,856,438 , GRCh38.p12 chr3: 112,137,591-112,137,591 , GRCh38.p12 chr3|NW_019805492.1: 20,881-20,881 0
    nsv6294285mobile element insertion1nstd186human GRCh37 chr3: 112,017,087-112,017,138 , GRCh38.p12 chr3: 112,298,240-112,298,291 , GRCh38.p12 chr3|NW_019805492.1: 190,978-191,029 0
    nsv6292004mobile element insertion1nstd186human GRCh37 chr3: 112,013,589-112,013,640 , GRCh38.p12 chr3|NW_019805492.1: 187,480-187,531 , GRCh38.p12 chr3: 112,294,742-112,294,793 SLC9C1
    nsv4806769copy number variation1nstd200human GRCh37 chr3: 111,957,128-111,976,052 , GRCh38.p12 chr3: 112,238,281-112,257,205 , GRCh38.p12 chr3|NW_019805492.1: 131,019-149,943 SLC9C1, LOC100532749
    nsv4806768copy number variation1nstd200human GRCh37 chr3: 111,954,897-111,955,823 , GRCh38.p12 chr3|NW_019805492.1: 128,788-129,714 , GRCh38.p12 chr3: 112,236,050-112,236,976 SLC9C1
    nsv4806767copy number variation1nstd200human GRCh37 chr3: 111,921,934-111,922,235 , GRCh38.p12 chr3: 112,203,087-112,203,388 , GRCh38.p12 chr3|NW_019805492.1: 95,825-96,126 SLC9C1
    nsv4806766copy number variation1nstd200human GRCh37 chr3: 111,862,164-111,863,566 , GRCh38.p12 chr3: 112,143,317-112,144,719 , GRCh38.p12 chr3|NW_019805492.1: 26,607-28,009 SLC9C1
    nsv4806765copy number variation1nstd200human GRCh37 chr3: 111,839,875-111,846,365 , GRCh38.p12 chr3|NW_019805492.1: 4,318-10,808 , GRCh38.p12 chr3: 112,121,028-112,127,518 GCSAM, C3orf52
    nsv4757081insertion1nstd199human GRCh37 chr3: 111,924,473-111,924,473 , GRCh38.p12 chr3|NW_019805492.1: 98,364-98,364 , GRCh38.p12 chr3: 112,205,626-112,205,626 SLC9C1
    nsv4587014copy number variation1nstd183human GRCh37 chr3: 111,851,817-111,923,659 , GRCh38.p12 chr3: 112,132,970-112,204,812 , GRCh38.p12 chr3|NW_019805492.1: 16,260-97,550 INAVAP1, TBILA, 3 more genes
    nsv4584661copy number variation1nstd183human GRCh37 chr3: 111,982,791-111,985,180 , GRCh38.p12 chr3|NW_019805492.1: 156,682-159,071 , GRCh38.p12 chr3: 112,263,944-112,266,333 SLC9C1
    nsv4584660copy number variation1nstd183human GRCh37 chr3: 111,921,162-111,923,032 , GRCh38.p12 chr3|NW_019805492.1: 95,053-96,923 , GRCh38.p12 chr3: 112,202,315-112,204,185 SLC9C1
    nsv4569333mobile element insertion1nstd166human GRCh37.p13 chr3: 111,921,156-111,921,156 , GRCh38.p12 chr3: 112,202,309-112,202,309 , GRCh38.p12 chr3|NW_019805492.1: 95,047-95,047 SLC9C1
    nsv4569258mobile element insertion1nstd166human GRCh37.p13 chr3: 111,941,929-111,941,929 , GRCh38.p12 chr3|NW_019805492.1: 115,820-115,820 , GRCh38.p12 chr3: 112,223,082-112,223,082 SLC9C1
    nsv4557763sequence alteration1nstd166human GRCh37.p13 chr3: 111,980,371-111,982,650 , GRCh38.p12 chr3|NW_019805492.1: 154,262-156,541 , GRCh38.p12 chr3: 112,261,524-112,263,803 SLC9C1
    nsv4552808insertion1nstd166human GRCh37.p13 chr3: 111,927,631-111,927,631 , GRCh38.p12 chr3|NW_019805492.1: 101,522-101,522 , GRCh38.p12 chr3: 112,208,784-112,208,784 SLC9C1
    nsv4552670insertion1nstd166human GRCh37.p13 chr3: 112,013,579-112,013,579 , GRCh38.p12 chr3|NW_019805492.1: 187,470-187,470 , GRCh38.p12 chr3: 112,294,732-112,294,732 SLC9C1
    nsv4552657insertion1nstd166human GRCh37.p13 chr3: 111,905,917-111,905,917 , GRCh38.p12 chr3|NW_019805492.1: 79,808-79,808 , GRCh38.p12 chr3: 112,187,070-112,187,070 SLC9C1
    nsv4468543mobile element insertion1nstd166human GRCh37.p13 chr3: 112,019,577-112,019,577 , GRCh38.p12 chr3|NW_019805492.1: 193,468-193,468 , GRCh38.p12 chr3: 112,300,730-112,300,730 LOC105374042
    nsv4468542mobile element insertion1nstd166human GRCh37.p13 chr3: 111,943,449-111,943,449 , GRCh38.p12 chr3: 112,224,602-112,224,602 , GRCh38.p12 chr3|NW_019805492.1: 117,340-117,340 SLC9C1
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