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 430

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055649inversion1nstd229human GRCh38 chr7: 53,073,992-53,978,957 , GRCh37.p13 chr7: 53,141,685-54,046,650 HAUS6P3, HAUS6P1, 9 more genes
    nsv7046217inversion1nstd229human GRCh38 chr7: 53,505,960-54,047,685 , GRCh37.p13 chr7: 53,573,653-54,115,378 RAC1P9, HAUS6P3, 4 more genes
    nsv7040097inversion1nstd229human GRCh38 chr7: 53,193,121-54,035,928 , GRCh37.p13 chr7: 53,260,814-54,103,621 LINC02854, RN7SKP218, 8 more genes
    nsv6837394copy number variation1nstd229human GRCh38 chr7: 53,742,068-53,742,107 , GRCh37.p13 chr7: 53,809,761-53,809,800 LINC01446
    nsv6836722copy number variation1nstd229human GRCh38 chr7: 51,354,950-55,353,996 , GRCh37.p13 chr7: 51,422,647-55,421,689 GS1-278J22.2, RNF138P2, 41 more genes
    nsv6835421copy number variation1nstd229human GRCh38 chr7: 53,686,759-53,841,190 , GRCh37.p13 chr7: 53,754,452-53,908,883 RAC1P9, RNU2-29P, 1 more genes
    nsv6834747copy number variation1nstd229human GRCh38 chr7: 53,183,701-53,884,000 , GRCh37.p13 chr7: 53,251,394-53,951,693 RNF138P2, GS1-278J22.2, 8 more genes
    nsv6833904copy number variation1nstd229human GRCh38 chr7: 53,736,457-53,741,664 , GRCh37.p13 chr7: 53,804,150-53,809,357 LINC01446
    nsv6833872copy number variation1nstd229human GRCh38 chr7: 53,760,532-53,763,659 , GRCh37.p13 chr7: 53,828,225-53,831,352 LINC01446
    nsv6831892copy number variation1nstd229human GRCh38 chr7: 53,693,101-53,695,100 , GRCh37.p13 chr7: 53,760,794-53,762,793 LINC01446
    nsv6831882copy number variation1nstd229human GRCh38 chr7: 53,663,820-53,665,431 , GRCh37.p13 chr7: 53,731,513-53,733,124 LINC01446
    nsv6831820copy number variation1nstd229human GRCh38 chr7: 53,680,557-53,709,834 , GRCh37.p13 chr7: 53,748,250-53,777,527 LINC01446
    nsv6831318copy number variation1nstd229human GRCh38 chr7: 53,809,463-53,813,730 , GRCh37.p13 chr7: 53,877,156-53,881,423 LINC01446
    nsv6830798copy number variation1nstd229human GRCh38 chr7: 53,760,755-53,761,540 , GRCh37.p13 chr7: 53,828,448-53,829,233 LINC01446
    nsv6830097copy number variation1nstd229human GRCh38 chr7: 53,651,159-53,678,647 , GRCh37.p13 chr7: 53,718,852-53,746,340 LINC01446
    nsv6827942copy number variation1nstd229human GRCh38 chr7: 53,624,742-53,654,897 , GRCh37.p13 chr7: 53,692,435-53,722,590 LINC01446
    nsv6825760copy number variation1nstd229human GRCh38 chr7: 53,679,342-53,679,374 , GRCh37.p13 chr7: 53,747,035-53,747,067 LINC01446
    nsv6824960copy number variation1nstd229human GRCh38 chr7: 53,711,699-53,719,806 , GRCh37.p13 chr7: 53,779,392-53,787,499 LINC01446
    nsv6824279copy number variation1nstd229human GRCh38 chr7: 53,679,234-53,798,079 , GRCh37.p13 chr7: 53,746,927-53,865,772 LINC01446, RNU2-29P, 1 more genes
    nsv6823714copy number variation1nstd229human GRCh38 chr7: 53,789,944-53,793,703 , GRCh37.p13 chr7: 53,857,637-53,861,396 LINC01446
    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