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 202

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129114copy number variation1nstd186human GRCh37 chr17: 8,246,653-8,247,968 , GRCh38.p12 chr17: 8,343,335-8,344,650 ODF4
    nsv5945739copy number variation1nstd209human GRCh38 chr17: 8,343,293-8,344,649 , GRCh37.p13 chr17: 8,246,611-8,247,967 ODF4
    nsv5939842copy number variation1nstd209human GRCh38 chr17: 8,342,887-8,344,667 , GRCh37.p13 chr17: 8,246,205-8,247,985 ODF4
    nsv5932247copy number variation1nstd209human GRCh38 chr17: 8,342,820-8,343,219 , GRCh37.p13 chr17: 8,246,138-8,246,537 ODF4
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5883039copy number variation1nstd209human GRCh38 chr17: 8,343,319-8,344,652 , GRCh37.p13 chr17: 8,246,637-8,247,970 ODF4
    nsv5604059copy number variation1nstd207human GRCh38 chr17: 8,343,293-8,344,649 , GRCh37.p13 chr17: 8,246,611-8,247,967 ODF4
    nsv5564399copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,192,101-8,283,260 , GRCh38.p12 chr17: 8,288,783-8,379,942 RANGRF, KRBA2, 5 more genes
    nsv5525019copy number variation1nstd206human GRCh38 chr17: 8,305,883-8,356,856 , GRCh37.p13 chr17: 8,209,201-8,260,174 ARHGEF15, ODF4, 1 more genes
    nsv5523853copy number variation1nstd206human GRCh38 chr17: 8,343,273-8,344,691 , GRCh37.p13 chr17: 8,246,591-8,248,009 ODF4
    nsv5519476copy number variation1nstd206human GRCh38 chr17: 8,342,847-8,343,220 , GRCh37.p13 chr17: 8,246,165-8,246,538 ODF4
    nsv5393207copy number variation1nstd186human GRCh37 chr17: 8,246,163-8,247,969 , GRCh38.p12 chr17: 8,342,845-8,344,651 ODF4
    nsv5392590copy number variation1nstd186human GRCh37 chr17: 8,246,705-8,247,472 , GRCh38.p12 chr17: 8,343,387-8,344,154 ODF4
    nsv5392310copy number variation1nstd186human GRCh37 chr17: 8,246,712-8,247,686 , GRCh38.p12 chr17: 8,343,394-8,344,368 ODF4
    nsv5392290copy number variation1nstd186human GRCh37 chr17: 8,247,121-8,247,485 , GRCh38.p12 chr17: 8,343,803-8,344,167 ODF4
    nsv5391497copy number variation1nstd186human GRCh37 chr17: 8,246,164-8,247,968 , GRCh38.p12 chr17: 8,342,846-8,344,650 ODF4
    nsv5391341copy number variation1nstd186human GRCh37 chr17: 8,246,890-8,247,861 , GRCh38.p12 chr17: 8,343,572-8,344,543 ODF4
    nsv5391065copy number variation1nstd186human GRCh37 chr17: 8,246,665-8,247,967 , GRCh38.p12 chr17: 8,343,347-8,344,649 ODF4
    nsv5300613copy number variation1nstd204human GRCh38.p13 chr17: 8,343,190-8,344,764 , GRCh37.p13 chr17: 8,246,508-8,248,082 ODF4
    nsv5296602copy number variation1nstd204human GRCh38.p13 chr17: 8,343,319-8,344,652 , GRCh37.p13 chr17: 8,246,637-8,247,970 ODF4
    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