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 605

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130721insertion1nstd186human GRCh37 chr17: 16,248,725-16,248,725 , GRCh38.p12 chr17: 16,345,411-16,345,411 PIGL, CENPV
    nsv6127083copy number variation1nstd186human GRCh37 chr17: 16,248,589-16,248,725 , GRCh38.p12 chr17: 16,345,275-16,345,411 CENPV, PIGL
    nsv5979534insertion1nstd209human GRCh38 chr17: 16,334,596-16,334,596 , GRCh37.p13 chr17: 16,237,910-16,237,910 PIGL
    nsv5977447insertion1nstd209human GRCh38 chr17: 16,216,786-16,216,786 , GRCh37.p13 chr17: 16,120,100-16,120,100 NCOR1, PIGL
    nsv5977405insertion1nstd209human GRCh38 chr17: 16,345,411-16,345,411 , GRCh37.p13 chr17: 16,248,725-16,248,725 PIGL, CENPV
    nsv5977246insertion1nstd209human GRCh38 chr17: 16,330,606-16,330,606 , GRCh37.p13 chr17: 16,233,920-16,233,920 PIGL
    nsv5975071insertion1nstd209human GRCh38 chr17: 16,219,580-16,219,580 , GRCh37.p13 chr17: 16,122,894-16,122,894 PIGL
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5970390insertion1nstd209human GRCh38 chr17: 16,311,467-16,311,467 , GRCh37.p13 chr17: 16,214,781-16,214,781 PIGL
    nsv5967762insertion1nstd209human GRCh38 chr17: 16,320,222-16,320,222 , GRCh37.p13 chr17: 16,223,536-16,223,536 PIGL
    nsv5945891copy number variation1nstd209human GRCh38 chr17: 15,750,946-16,668,217 , GRCh37.p13 chr17: 15,654,260-16,571,531 ADORA2B, MIR1288, 34 more genes
    nsv5945358copy number variation1nstd209human GRCh38 chr17: 16,264,203-16,264,335 , GRCh37.p13 chr17: 16,167,517-16,167,649 PIGL
    nsv5944498copy number variation1nstd209human GRCh38 chr17: 16,251,501-16,251,807 , GRCh37.p13 chr17: 16,154,815-16,155,121 PIGL
    nsv5943631copy number variation1nstd209human GRCh38 chr17: 15,758,933-16,863,323 , GRCh37.p13 chr17: 15,662,247-16,766,637 , MIR1288, 50 more genes
    nsv5941172copy number variation1nstd209human GRCh38 chr17: 16,301,378-16,303,651 , GRCh37.p13 chr17: 16,204,692-16,206,965 PIGL
    nsv5940764copy number variation1nstd209human GRCh38 chr17: 15,758,291-16,862,696 , GRCh37.p13 chr17: 15,661,605-16,766,010 , ZSWIM5P1, 50 more genes
    nsv5934886copy number variation1nstd209human GRCh38 chr17: 16,333,403-16,338,142 , GRCh37.p13 chr17: 16,236,717-16,241,456 PIGL
    nsv5931210copy number variation1nstd209human GRCh38 chr17: 16,299,261-16,300,486 , GRCh37.p13 chr17: 16,202,575-16,203,800 PIGL
    nsv5930836copy number variation1nstd209human GRCh38 chr17: 16,306,054-16,310,641 , GRCh37.p13 chr17: 16,209,368-16,213,955 PIGL
    nsv5930324copy number variation1nstd209human GRCh38 chr17: 16,312,089-16,312,141 , GRCh37.p13 chr17: 16,215,403-16,215,455 PIGL
    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