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 203

    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
    nsv6937156copy number variation1nstd229human GRCh38 chr13: 19,021,517-19,071,823 , GRCh37.p13 chr13: 19,595,657-19,645,963 PHF2P1, GTF2IP3
    nsv6936926copy number variation1nstd229human GRCh38 chr13: 19,047,851-19,072,504 , GRCh37.p13 chr13: 19,621,991-19,646,644 LOC107984132, PHF2P1
    nsv6936078copy number variation1nstd229human GRCh38 chr13: 19,043,543-19,046,631 , GRCh37.p13 chr13: 19,617,683-19,620,771 PHF2P1
    nsv6934876copy number variation1nstd229human GRCh38 chr13: 18,983,674-19,141,312 , GRCh37.p13 chr13: 19,557,814-19,715,452 CENPIP1, RNA5SP24, 6 more genes
    nsv6934000copy number variation1nstd229human GRCh38 chr13: 19,053,437-19,058,475 , GRCh37.p13 chr13: 19,627,577-19,632,615 PHF2P1
    nsv6928152copy number variation1nstd229human GRCh38 chr13: 19,047,837-19,056,049 , GRCh37.p13 chr13: 19,621,977-19,630,189 PHF2P1
    nsv6926048copy number variation1nstd229human GRCh38 chr13: 19,049,985-19,053,834 , GRCh37.p13 chr13: 19,624,125-19,627,974 PHF2P1
    nsv6922379copy number variation1nstd229human GRCh38 chr13: 19,044,058-19,056,123 , GRCh37.p13 chr13: 19,618,198-19,630,263 PHF2P1
    nsv6921512copy number variation1nstd229human GRCh38 chr13: 19,022,301-19,120,000 , GRCh37.p13 chr13: 19,596,441-19,694,140 RNA5SP24, LOC107984132, 2 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
    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
    nsv6622113copy number variation1nstd224human GRCh37 chr13: 19,596,992-19,640,445 , GRCh38.p12 chr13: 19,022,852-19,066,305 PHF2P1, GTF2IP3
    nsv6622112copy number variation2nstd224human GRCh37 chr13: 19,541,688-19,622,143 , GRCh38.p12 chr13: 18,967,548-19,048,003 LINC00442, PHF2P1, 2 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
    nsv6581171inversion1nstd223human GRCh38 chr13: 19,051,674-20,424,294 , GRCh37.p13 chr13: 19,625,814-20,998,433 RN7SL166P, PARP4P2, 35 more genes
    nsv6493415copy number variation1nstd223human GRCh38 chr13: 18,983,681-19,141,293 , GRCh37.p13 chr13: 19,557,821-19,715,433 PHF2P1, LINC00442, 6 more genes
    nsv6486785copy number variation1nstd223human GRCh38 chr13: 19,044,058-19,056,120 , GRCh37.p13 chr13: 19,618,198-19,630,260 PHF2P1
    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