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 145

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073674inversion1nstd229human GRCh38 chr13: 19,051,673-20,424,293 , GRCh37.p13 chr13: 19,625,813-20,998,432 ST6GALNAC4P1, LINC01072, 35 more genes
    nsv7071280inversion1nstd229human GRCh38 chr13: 19,060,302-19,582,752 , GRCh37.p13 chr13: 19,634,442-20,156,892 ESRRAP1, GOLM2P1, 18 more genes
    nsv7071034inversion1nstd229human GRCh38 chr13: 19,239,514-24,381,508 , GRCh37.p13 chr13: 19,813,654-24,955,646 BASP1P1, ZMYM5, 111 more genes
    nsv7069596inversion1nstd229human GRCh38 chr13: 19,338,874-19,796,660 , GRCh37.p13 chr13: 19,913,014-20,370,800 SLC25A15P2, MRPS31P2, 12 more genes
    nsv6936987copy number variation1nstd229human GRCh38 chr13: 19,345,830-19,345,895 , GRCh37.p13 chr13: 19,919,970-19,920,035 LINC00421
    nsv6930481copy number variation1nstd229human GRCh38 chr13: 19,296,501-20,027,300 , GRCh37.p13 chr13: 19,870,641-20,601,440 ZMYM5, LINC00421, 16 more genes
    nsv6929363copy number variation1nstd229human GRCh38 chr13: 19,343,501-19,694,600 , GRCh37.p13 chr13: 19,917,641-20,268,740 GOLM2P1, MRPS31P2, 11 more genes
    nsv6924593copy number variation1nstd229human GRCh38 chr13: 19,243,454-19,710,588 , GRCh37.p13 chr13: 19,817,594-20,284,728 MRPL3P1, MRPS31P2, 12 more genes
    nsv6923155copy number variation1nstd229human GRCh38 chr13: 19,301,769-19,710,590 , GRCh37.p13 chr13: 19,875,909-20,284,730 TPTE2, ESRRAP1, 12 more genes
    nsv6637646copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,287-22,089,005 , GRCh38.p12 chr13: 18,862,147-21,514,866 LOC105370104, RNU6-52P, 78 more genes
    nsv6637564copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,725,083-20,273,635 , GRCh38.p12 chr13: 19,150,943-19,699,495 TPTE2, CYCSP32, 16 more genes
    nsv6637390copy number variation1nstd102humanUncertain significance GRCh37 chr13: 19,436,287-22,405,375 , GRCh38.p12 chr13: 18,862,147-21,831,236 SLC35E1P1, LOC107984553, 83 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6621660copy number variation1nstd224human GRCh37 chr13: 19,857,865-19,993,564 , GRCh38.p12 chr13: 19,283,725-19,419,424 MRPL3P1, PARP4P2, 4 more genes
    nsv6621657copy number variation1nstd224human GRCh37 chr13: 19,121,950-20,440,020 , GRCh38.p12 chr13: 18,547,810-19,865,880 TERF1P5, MRPS31P2, 46 more genes
    nsv6584962inversion1nstd223human GRCh38 chr13: 19,190,117-21,198,044 , GRCh37.p13 chr13: 19,764,257-21,772,183 GOLM2P1, ANKRD26P3, 49 more genes
    nsv6581171inversion1nstd223human GRCh38 chr13: 19,051,674-20,424,294 , GRCh37.p13 chr13: 19,625,814-20,998,433 RN7SL166P, PARP4P2, 35 more genes
    nsv6489897copy number variation1nstd223human GRCh38 chr13: 19,243,450-19,710,588 , GRCh37.p13 chr13: 19,817,590-20,284,728 MRPL3P1, GOLM2P1, 12 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 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