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 358

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139784copy number variation1nstd232human GRCh37.p13 chr1: 171,492,491-171,492,570 , GRCh38.p12 chr1: 171,523,352-171,523,431 PRRC2C
    nsv6644765copy number variation1nstd229human GRCh38 chr1: 171,564,330-172,954,419 , GRCh37.p13 chr1: 171,533,469-172,923,559 LOC107985225, RPS15P3, 27 more genes
    nsv6644690copy number variation1nstd229human GRCh38 chr1: 171,488,019-171,488,063 , GRCh37.p13 chr1: 171,457,158-171,457,202 PRRC2C
    nsv6644316copy number variation1nstd229human GRCh38 chr1: 171,527,600-171,527,653 , GRCh37.p13 chr1: 171,496,739-171,496,792 PRRC2C
    nsv6636536copy number variation1nstd102humanUncertain significance GRCh37 chr1: 171,186,446-171,907,499 , GRCh38.p12 chr1: 171,217,307-171,938,359 METTL13, MYOC, 22 more genes
    nsv6552013inversion1nstd223human GRCh38 chr1: 171,483,594-171,484,154 , GRCh37.p13 chr1: 171,452,733-171,453,293 PRRC2C
    nsv6549844inversion1nstd223human GRCh38 chr1: 171,527,251-171,527,557 , GRCh37.p13 chr1: 171,496,390-171,496,696 PRRC2C
    nsv6546833inversion1nstd223human GRCh38 chr1: 171,578,002-171,578,686 , GRCh37.p13 chr1: 171,547,141-171,547,825 PRRC2C
    nsv6539645inversion1nstd223human GRCh38 chr1: 171,502,741-171,503,419 , GRCh37.p13 chr1: 171,471,880-171,472,558 PRRC2C
    nsv6335442copy number variation1nstd223human GRCh38 chr1: 171,526,499-171,527,366 , GRCh37.p13 chr1: 171,495,638-171,496,505 PRRC2C
    nsv6334464copy number variation1nstd223human GRCh38 chr1: 171,581,376-171,581,778 , GRCh37.p13 chr1: 171,550,515-171,550,917 PRRC2C
    nsv6334195copy number variation1nstd223human GRCh38 chr1: 171,527,231-171,528,330 , GRCh37.p13 chr1: 171,496,370-171,497,469 PRRC2C
    nsv6322142copy number variation1nstd223human GRCh38 chr1: 171,582,252-171,583,411 , GRCh37.p13 chr1: 171,551,391-171,552,550 PRRC2C
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6295571copy number variation1nstd186human GRCh37 chr1: 171,475,665-171,475,746 , GRCh38.p12 chr1: 171,506,526-171,506,607 PRRC2C
    nsv6133941copy number variation1nstd213human GRCh37 chr1: 171,410,000-171,700,001 , GRCh38.p12 chr1: 171,440,861-171,730,861 MYOC, VAMP4, 6 more genes
    nsv6133940copy number variation1nstd213human GRCh37 chr1: 170,740,000-173,330,001 , GRCh38.p12 chr1: 170,770,859-173,360,862 TNFSF4, VAMP4, 50 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 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