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Items: 1 to 20 of 150

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6642744copy number variation1nstd229human GRCh38 chr1: 156,008,846-156,009,638 , GRCh37.p13 chr1: 155,978,637-155,979,429 SSR2
    nsv6642529copy number variation1nstd229human GRCh38 chr1: 155,983,660-156,013,131 , GRCh37.p13 chr1: 155,953,451-155,982,922 ARHGEF2, SSR2, 1 more genes
    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
    nsv6642293copy number variation1nstd229human GRCh38 chr1: 156,020,233-156,022,194 , GRCh37.p13 chr1: 155,990,024-155,991,985 SSR2, LOC105371729
    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
    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
    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
    nsv6317671copy number variation1nstd223human GRCh38 chr1: 156,009,526-156,058,387 , GRCh37.p13 chr1: 155,979,317-156,028,178 LOC105371729, UBQLN4, 2 more genes
    nsv6317340copy number variation1nstd223human GRCh38 chr1: 156,014,801-156,016,900 , GRCh37.p13 chr1: 155,984,592-155,986,691 SSR2
    nsv6316196copy number variation1nstd223human GRCh38 chr1: 156,017,848-156,028,742 , GRCh37.p13 chr1: 155,987,639-155,998,533 SSR2, LOC105371729
    nsv6313583copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,616,264-156,059,947 , GRCh38.p12 chr1: 155,646,473-156,090,156 ARHGEF2-AS2, MIR6738, 26 more genes
    nsv6310682copy number variation1nstd102humanUncertain significance GRCh37 chr1: 155,870,179-156,146,788 , GRCh38.p12 chr1: 155,900,388-156,176,997 LOC105371729, SNORA80E, 16 more genes
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310593copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,581,953-156,851,434 , GRCh38.p12 chr1: 155,612,162-156,881,642 MIR9-1, MRPL24, 62 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6296184copy number variation1nstd186human GRCh37 chr1: 155,987,302-155,987,702 , GRCh38.p12 chr1: 156,017,511-156,017,911 SSR2
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