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 379

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074210inversion1nstd229human GRCh38 chr18: 45,861,287-52,164,943 , GRCh37.p13 chr18: 43,441,252-49,691,313 LOC105372100, RNA5SP458, 103 more genes
    nsv7058348inversion1nstd229human GRCh38 chr18: 49,550,777-51,013,398 , GRCh37.p13 chr18: 47,077,147-48,539,768 SMUG1P1, CXXC1, 26 more genes
    nsv7015620copy number variation1nstd229human GRCh38 chr18: 48,566,814-53,963,212 , GRCh37.p13 chr18: 46,093,185-51,489,582 LINC02837, RPL29P32, 65 more genes
    nsv7015023copy number variation1nstd229human GRCh38 chr18: 50,946,498-50,950,776 , GRCh37.p13 chr18: 48,472,868-48,477,146 ME2
    nsv7009635copy number variation1nstd229human GRCh38 chr18: 50,945,701-50,974,400 , GRCh37.p13 chr18: 48,472,071-48,500,770 ELAC1, ME2
    nsv7008821copy number variation1nstd229human GRCh38 chr18: 50,907,224-50,907,564 , GRCh37.p13 chr18: 48,433,594-48,433,934 ME2
    nsv7008434copy number variation1nstd229human GRCh38 chr18: 50,899,912-50,902,250 , GRCh37.p13 chr18: 48,426,282-48,428,620 ME2
    nsv7007544copy number variation1nstd229human GRCh38 chr18: 50,919,489-50,930,251 , GRCh37.p13 chr18: 48,445,859-48,456,621 ME2
    nsv7003570copy number variation1nstd229human GRCh38 chr18: 50,884,950-51,036,179 , GRCh37.p13 chr18: 48,411,320-48,562,549 LOC107985152, ME2, 2 more genes
    nsv7001708copy number variation1nstd229human GRCh38 chr18: 50,813,388-50,881,372 , GRCh37.p13 chr18: 48,339,758-48,407,742 MRO, HNRNPA3P16, 2 more genes
    nsv7000130copy number variation1nstd229human GRCh38 chr18: 50,902,683-50,903,047 , GRCh37.p13 chr18: 48,429,053-48,429,417 ME2
    nsv6998106copy number variation1nstd229human GRCh38 chr18: 50,894,069-50,894,258 , GRCh37.p13 chr18: 48,420,439-48,420,628 ME2
    nsv6637893copy number variation1nstd102humanUncertain significance GRCh37 chr18: 48,273,185-51,134,173 , GRCh38.p12 chr18: 50,746,815-53,607,803 LOC105372121, LOC100420949, 23 more genes
    nsv6595020inversion1nstd223human GRCh38 chr18: 49,148,101-52,144,680 , GRCh37.p13 chr18: 46,674,471-49,671,050 MYO5B, LIPG, 49 more genes
    nsv6590038inversion1nstd223human GRCh38 chr18: 50,927,447-50,928,066 , GRCh37.p13 chr18: 48,453,817-48,454,436 ME2
    nsv6586029inversion1nstd223human GRCh38 chr18: 50,886,319-50,886,887 , GRCh37.p13 chr18: 48,412,689-48,413,257 ME2
    nsv6584582inversion1nstd223human GRCh38 chr18: 50,945,283-50,945,817 , GRCh37.p13 chr18: 48,471,653-48,472,187 ME2
    nsv6577857inversion1nstd223human GRCh38 chr18: 50,940,917-50,941,681 , GRCh37.p13 chr18: 48,467,287-48,468,051 ME2
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 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