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 285

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7059192inversion1nstd229human GRCh38 chr17: 30,069,297-30,546,697 , GRCh37.p13 chr17: 28,396,315-28,873,715 SLC6A4, LOC105371720, 13 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6994356copy number variation1nstd229human GRCh38 chr17: 30,181,943-30,206,905 , GRCh37.p13 chr17: 28,508,961-28,533,923 NSRP1, SLC6A4
    nsv6993595copy number variation1nstd229human GRCh38 chr17: 30,148,591-30,178,689 , GRCh37.p13 chr17: 28,475,609-28,505,707 NSRP1
    nsv6987583copy number variation1nstd229human GRCh38 chr17: 30,180,841-30,180,871 , GRCh37.p13 chr17: 28,507,859-28,507,889 NSRP1
    nsv6987060copy number variation1nstd229human GRCh38 chr17: 30,158,455-30,161,560 , GRCh37.p13 chr17: 28,485,473-28,488,578 NSRP1
    nsv6986814copy number variation1nstd229human GRCh38 chr17: 30,180,103-30,210,437 , GRCh37.p13 chr17: 28,507,121-28,537,455 NSRP1, SLC6A4
    nsv6983791copy number variation1nstd229human GRCh38 chr17: 30,123,053-30,123,123 , GRCh37.p13 chr17: 28,450,071-28,450,141 NSRP1
    nsv6983748copy number variation1nstd229human GRCh38 chr17: 30,139,098-30,139,187 , GRCh37.p13 chr17: 28,466,116-28,466,205 NSRP1
    nsv6982880copy number variation1nstd229human GRCh38 chr17: 30,114,601-30,117,000 , GRCh37.p13 chr17: 28,441,619-28,444,018 MIR3184, MIR423, 1 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6978581copy number variation1nstd229human GRCh38 chr17: 30,041,301-30,206,800 , GRCh37.p13 chr17: 28,368,319-28,533,818 SLC6A4, EFCAB5, 5 more genes
    nsv6587451inversion1nstd223human GRCh38 chr17: 30,149,707-30,150,100 , GRCh37.p13 chr17: 28,476,725-28,477,118 NSRP1
    nsv6579712inversion1nstd223human GRCh38 chr17: 30,181,606-30,182,930 , GRCh37.p13 chr17: 28,508,624-28,509,948 NSRP1
    nsv6578793inversion1nstd223human GRCh38 chr17: 30,125,190-30,125,571 , GRCh37.p13 chr17: 28,452,208-28,452,589 NSRP1
    nsv6577059inversion1nstd223human GRCh38 chr17: 30,175,466-30,175,991 , GRCh37.p13 chr17: 28,502,484-28,503,009 NSRP1
    nsv6515587copy number variation1nstd223human GRCh38 chr17: 30,138,996-30,139,187 , GRCh37.p13 chr17: 28,466,014-28,466,205 NSRP1
    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