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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095755copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 155,581,953-155,880,552 , GRCh38.p12 chr1: 155,612,162-155,910,761 SYT11, RIT1, 12 more genes
    nsv7055468inversion1nstd229human GRCh38 chr1: 155,667,181-158,101,472 , GRCh37.p13 chr1: 155,636,972-158,071,262 FCRL4, CRABP2, 88 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6642739copy number variation1nstd229human GRCh38 chr1: 155,869,870-155,872,697 , GRCh37.p13 chr1: 155,839,661-155,842,488 SYT11
    nsv6642614copy number variation1nstd229human GRCh38 chr1: 155,874,563-155,875,221 , GRCh37.p13 chr1: 155,844,354-155,845,012 SYT11
    nsv6642613copy number variation1nstd229human GRCh38 chr1: 155,866,379-155,867,094 , GRCh37.p13 chr1: 155,836,170-155,836,885 SYT11
    nsv6642525copy number variation1nstd229human GRCh38 chr1: 155,885,501-156,538,600 , GRCh37.p13 chr1: 155,855,292-156,508,392 TMEM79, MEF2D, 33 more genes
    nsv6642524copy number variation1nstd229human GRCh38 chr1: 155,859,444-155,859,511 , GRCh37.p13 chr1: 155,829,235-155,829,302 GON4L, SYT11
    nsv6642285copy number variation1nstd229human GRCh38 chr1: 155,874,478-155,875,220 , GRCh37.p13 chr1: 155,844,269-155,845,011 SYT11
    nsv6637136copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,489,474-156,196,407 , GRCh38.p12 chr1: 155,519,683-156,226,616 YY1AP1, ASH1L, 37 more genes
    nsv6549694inversion1nstd223human GRCh38 chr1: 155,298,173-158,468,085 , GRCh37.p13 chr1: 155,267,964-158,437,875 ASH1L, GPATCH4, 121 more genes
    nsv6536519inversion1nstd223human GRCh38 chr1: 155,864,729-155,865,644 , GRCh37.p13 chr1: 155,834,520-155,835,435 SYT11
    nsv6329729copy number variation1nstd223human GRCh38 chr1: 155,877,087-155,877,585 , GRCh37.p13 chr1: 155,846,878-155,847,376 SYT11
    nsv6329527copy number variation1nstd223human GRCh38 chr1: 155,481,601-157,146,700 , GRCh37.p13 chr1: 155,451,392-157,116,492 BGLAP, SSR2, 78 more genes
    nsv6328270copy number variation1nstd223human GRCh38 chr1: 155,870,997-155,872,385 , GRCh37.p13 chr1: 155,840,788-155,842,176 SYT11
    nsv6324654copy number variation1nstd223human GRCh38 chr1: 155,874,472-155,875,220 , GRCh37.p13 chr1: 155,844,263-155,845,011 SYT11
    nsv6320960copy number variation1nstd223human GRCh38 chr1: 155,866,354-155,867,149 , GRCh37.p13 chr1: 155,836,145-155,836,940 SYT11
    nsv6319012copy number variation1nstd223human GRCh38 chr1: 155,567,801-156,556,900 , GRCh37.p13 chr1: 155,537,592-156,526,692 ARHGEF2-AS1, RAB25, 48 more genes
    nsv6318852copy number variation1nstd223human GRCh38 chr1: 155,842,452-155,874,751 , GRCh37.p13 chr1: 155,812,243-155,844,542 SYT11, GON4L, 1 more genes
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