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 246

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130684insertion1nstd186human GRCh37 chr22: 41,696,514-41,696,514 , GRCh38.p12 chr22: 41,300,510-41,300,510 ZC3H7B, RANGAP1
    nsv6129138insertion1nstd186human GRCh37 chr22: 41,710,941-41,710,979 , GRCh38.p12 chr22: 41,314,937-41,314,975 ZC3H7B
    nsv5974145insertion1nstd209human GRCh38 chr22: 41,314,924-41,314,924 , GRCh37.p13 chr22: 41,710,928-41,710,928 ZC3H7B
    nsv5967599insertion1nstd209human GRCh38 chr22: 41,300,480-41,300,480 , GRCh37.p13 chr22: 41,696,484-41,696,484 RANGAP1, ZC3H7B
    nsv5966908copy number variation1nstd209human GRCh38 chr22: 41,341,486-41,341,805 , GRCh37.p13 chr22: 41,737,490-41,737,809 ZC3H7B
    nsv5961677copy number variation1nstd209human GRCh38 chr22: 41,326,439-41,326,519 , GRCh37.p13 chr22: 41,722,443-41,722,523 ZC3H7B
    nsv5957793copy number variation1nstd209human GRCh38 chr22: 41,232,160-41,458,145 , GRCh37.p13 chr22: 41,628,164-41,854,149 ZC3H7B, LOC105373042, 9 more genes
    nsv5949379copy number variation1nstd209human GRCh38 chr22: 41,357,565-41,357,634 , GRCh37.p13 chr22: 41,753,569-41,753,638 ZC3H7B
    nsv5887551copy number variation2nstd209human GRCh38 chr22: 41,298,814-41,300,020 , GRCh37.p13 chr22: 41,694,818-41,696,024 RANGAP1, ZC3H7B
    nsv5886379copy number variation1nstd209human GRCh38 chr22: 41,316,588-41,336,920 , GRCh37.p13 chr22: 41,712,592-41,732,924 ZC3H7B
    nsv5871376copy number variation1nstd209human GRCh38 chr22: 41,296,814-41,303,172 , GRCh37.p13 chr22: 41,692,818-41,699,176 RANGAP1, ZC3H7B
    nsv5868241copy number variation1nstd209human GRCh38 chr22: 41,301,773-41,310,116 , GRCh37.p13 chr22: 41,697,777-41,706,120 ZC3H7B, RANGAP1
    nsv5704375mobile element insertion2nstd211human GRCh38 chr22: 41,314,937-41,314,937 , GRCh37.p13 chr22: 41,710,941-41,710,941 ZC3H7B
    nsv5669241insertion1nstd207human GRCh38 chr22: 41,300,510-41,300,510 , GRCh37.p13 chr22: 41,696,514-41,696,514 RANGAP1, ZC3H7B
    nsv5668518insertion1nstd207human GRCh38 chr22: 41,314,924-41,314,924 , GRCh37.p13 chr22: 41,710,928-41,710,928 ZC3H7B
    nsv5665712insertion1nstd207human GRCh38 chr22: 41,326,337-41,326,337 , GRCh37.p13 chr22: 41,722,341-41,722,341 ZC3H7B
    nsv5544381insertion1nstd206human GRCh38 chr22: 41,300,510-41,300,510 , GRCh37.p13 chr22: 41,696,514-41,696,514 ZC3H7B, RANGAP1
    nsv5534283insertion1nstd206human GRCh38 chr22: 41,314,937-41,314,975 , GRCh37.p13 chr22: 41,710,941-41,710,979 ZC3H7B
    nsv5293624copy number variation1nstd204human GRCh38.p13 chr22: 41,236,101-41,543,100 , GRCh37.p13 chr22: 41,632,105-41,939,104 LOC105373042, RANGAP1, 11 more genes
    nsv5281292copy number variation1nstd204human GRCh38.p13 chr22: 41,124,301-41,900,100 , GRCh37.p13 chr22: 41,520,305-42,296,104 SNU13, RANGAP1, 34 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