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 941

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136993copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 33,376,235-33,384,192 , GRCh38.p12 chr7: 33,336,623-33,344,580 BBS9
    nsv7098825copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,303,902-33,303,986 , GRCh38 chr7: 33,264,290-33,264,374 BBS9
    nsv7098117copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,376,033-33,427,776 , GRCh38.p12 chr7: 33,336,421-33,388,164 BBS9, LOC100421336
    nsv7097739copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,388,660-33,397,627 , GRCh38.p12 chr7: 33,349,048-33,358,015 BBS9
    nsv7097738copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,388,660-33,388,802 , GRCh38.p12 chr7: 33,349,048-33,349,190 BBS9
    nsv7097737copy number variation1nstd102humanUncertain significance GRCh37 chr7: 33,192,313-33,195,314 , GRCh38.p12 chr7: 33,152,701-33,155,702 BBS9
    nsv7097736copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 33,192,293-33,192,483 , GRCh38.p12 chr7: 33,152,681-33,152,871 BBS9
    nsv7097624copy number variation1nstd102humanUncertain significance GRCh37 chr7: 33,185,865-33,644,838 , GRCh38.p12 chr7: 33,146,253-33,605,226 LOC100421336, BBS9, 1 more genes
    nsv7097369copy number variation1nstd102humanUncertain significance GRCh37 chr7: 33,644,477-33,767,915 , GRCh38.p12 chr7: 33,604,865-33,728,303 BBS9, FLJ20712
    nsv7097368copy number variation1nstd102humanUncertain significance GRCh37 chr7: 33,217,070-34,888,295 , GRCh38.p12 chr7: 33,177,458-34,848,683 RN7SL132P, NPSR1, 9 more genes
    nsv7097367copy number variation1nstd102humanPathogenic GRCh37 chr7: 33,054,342-33,185,996 , GRCh38.p12 chr7: 33,014,730-33,146,384 BBS9, NT5C3A, 3 more genes
    nsv7047270inversion1nstd229human GRCh38 chr7: 33,179,763-33,182,907 , GRCh37.p13 chr7: 33,219,375-33,222,519 BBS9
    nsv7047251inversion1nstd229human GRCh38 chr7: 33,518,150-33,544,431 , GRCh37.p13 chr7: 33,557,762-33,584,043 BBS9
    nsv7041569inversion1nstd229human GRCh38 chr7: 33,154,293-33,154,454 , GRCh37.p13 chr7: 33,193,905-33,194,066 BBS9
    nsv7041324inversion1nstd229human GRCh38 chr7: 33,231,188-33,240,369 , GRCh37.p13 chr7: 33,270,800-33,279,981 BBS9
    nsv7038119inversion1nstd229human GRCh38 chr7: 33,231,480-33,236,803 , GRCh37.p13 chr7: 33,271,092-33,276,415 BBS9
    nsv6838048copy number variation1nstd229human GRCh38 chr7: 33,374,167-33,378,149 , GRCh37.p13 chr7: 33,413,779-33,417,761 LOC100421336, BBS9
    nsv6838047copy number variation1nstd229human GRCh38 chr7: 33,458,787-33,598,919 , GRCh37.p13 chr7: 33,498,399-33,638,531 BBS9
    nsv6837661copy number variation1nstd229human GRCh38 chr7: 33,410,557-33,419,805 , GRCh37.p13 chr7: 33,450,169-33,459,417 BBS9
    nsv6837344copy number variation1nstd229human GRCh38 chr7: 33,441,451-33,442,470 , GRCh37.p13 chr7: 33,481,063-33,482,082 BBS9
    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