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 195

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099251copy number variation1nstd231human GRCh38.p12 chr1: 177,558,975-179,087,722 , GRCh37 chr1: 177,528,110-179,056,857 ANGPTL1, RASAL2, 24 more genes
    nsv7053017inversion1nstd229human GRCh38 chr1: 177,759,800-179,689,836 , GRCh37.p13 chr1: 177,728,935-179,658,971 LOC105371630, TEX35, 39 more genes
    nsv7050782inversion1nstd229human GRCh38 chr1: 178,302,511-179,603,198 , GRCh37.p13 chr1: 178,271,646-179,572,333 PTPN2P1, MEF2AP1, 33 more genes
    nsv7044079inversion1nstd229human GRCh38 chr1: 174,711,171-179,623,233 , GRCh37.p13 chr1: 174,680,309-179,592,368 LOC100420262, RNU6-307P, 71 more genes
    nsv6645467copy number variation1nstd229human GRCh38 chr1: 178,487,448-178,487,500 , GRCh37.p13 chr1: 178,456,583-178,456,635 CLEC20A
    nsv6645417copy number variation1nstd229human GRCh38 chr1: 178,480,001-178,556,300 , GRCh37.p13 chr1: 178,449,136-178,525,435 TEX35, LOC105371631, 4 more genes
    nsv6644946copy number variation1nstd229human GRCh38 chr1: 178,489,666-178,496,640 , GRCh37.p13 chr1: 178,458,801-178,465,775 CLEC20A
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133835copy number variation1nstd213human GRCh37 chr1: 177,040,000-182,410,001 , GRCh38.p12 chr1: 177,070,864-182,440,866 VDAC1P4, RASAL2, 92 more genes
    nsv6133573copy number variation1nstd213human GRCh37 chr1: 173,820,000-189,960,001 , GRCh38.p12 chr1: 173,850,862-189,990,871 ABL2, ASTN1, 235 more genes
    nsv5681363mobile element insertion2nstd211human GRCh38 chr1: 178,478,163-178,478,163 , GRCh37.p13 chr1: 178,447,298-178,447,298 CLEC20A, RASAL2
    nsv5418309copy number variation1nstd206human GRCh38 chr1: 178,488,365-178,488,420 , GRCh37.p13 chr1: 178,457,500-178,457,555 CLEC20A
    nsv5401184mobile element insertion1nstd206human GRCh38 chr1: 178,478,163-178,478,199 , GRCh37.p13 chr1: 178,447,298-178,447,334 CLEC20A, RASAL2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv4898211copy number variation1nstd200human GRCh38 chr1: 178,499,105-178,500,317 , GRCh37.p13 chr1: 178,468,240-178,469,452 CLEC20A, LOC101928866
    nsv4898210copy number variation1nstd200human GRCh38 chr1: 178,496,983-178,499,173 , GRCh37.p13 chr1: 178,466,118-178,468,308 LOC101928866, CLEC20A
    nsv4784792copy number variation1nstd200human GRCh37 chr1: 178,468,240-178,469,452 , GRCh38.p12 chr1: 178,499,105-178,500,317 LOC101928866, CLEC20A
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 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