U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 135

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099236copy number variation1nstd231human GRCh38.p12 chr1: 156,064,931-157,804,884 , GRCh37 chr1: 156,034,722-157,774,674 BGLAP, CRABP2, 58 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
    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
    nsv6642295copy number variation1nstd229human GRCh38 chr1: 156,045,601-156,083,900 , GRCh37.p13 chr1: 156,015,392-156,053,691 UBQLN4, RAB25, 3 more genes
    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
    nsv6324448copy number variation1nstd223human GRCh38 chr1: 156,060,273-156,061,498 , GRCh37.p13 chr1: 156,030,064-156,031,289 RAB25
    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
    nsv6313660copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,034,721-156,240,338 , GRCh38.p12 chr1: 156,064,930-156,270,547 MEX3A, SLC25A44, 8 more genes
    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
    nsv6133588copy number variation1nstd213human GRCh37 chr1: 155,690,000-158,310,001 , GRCh38.p12 chr1: 155,720,209-158,340,211 CD1C, INSRR, 95 more genes
    nsv6133587copy number variation1nstd213human GRCh37 chr1: 155,490,000-156,310,001 , GRCh38.p12 chr1: 155,520,209-156,340,210 SSR2, SLC25A44, 45 more genes
    nsv6133562copy number variation1nstd213human GRCh37 chr1: 156,040,000-158,340,001 , GRCh38.p12 chr1: 156,070,209-158,370,211 CD1A, CD5L, 75 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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