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 304

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099250copy number variation1nstd231human GRCh38.p12 chr1: 174,623,673-177,335,804 , GRCh37 chr1: 174,592,811-177,304,940 ASTN1, TNR, 29 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
    nsv6645428copy number variation1nstd229human GRCh38 chr1: 177,277,133-177,278,393 , GRCh37.p13 chr1: 177,246,269-177,247,529 BRINP2
    nsv6645427copy number variation1nstd229human GRCh38 chr1: 177,276,995-177,278,402 , GRCh37.p13 chr1: 177,246,131-177,247,538 BRINP2
    nsv6645426copy number variation1nstd229human GRCh38 chr1: 177,226,201-177,230,800 , GRCh37.p13 chr1: 177,195,337-177,199,936 BRINP2
    nsv6645425copy number variation1nstd229human GRCh38 chr1: 177,196,387-177,214,410 , GRCh37.p13 chr1: 177,165,523-177,183,546 BRINP2
    nsv6645424copy number variation1nstd229human GRCh38 chr1: 177,190,547-177,193,276 , GRCh37.p13 chr1: 177,159,683-177,162,412 BRINP2
    nsv6645423copy number variation1nstd229human GRCh38 chr1: 177,161,968-177,170,372 , GRCh37.p13 chr1: 177,131,104-177,139,508 ASTN1, BRINP2
    nsv6645377copy number variation1nstd229human GRCh38 chr1: 177,200,161-177,211,725 , GRCh37.p13 chr1: 177,169,297-177,180,861 BRINP2
    nsv6645371copy number variation1nstd229human GRCh38 chr1: 177,069,160-177,304,928 , GRCh37.p13 chr1: 177,038,296-177,274,064 ASTN1, LOC105371625, 1 more genes
    nsv6644913copy number variation1nstd229human GRCh38 chr1: 177,181,846-177,182,007 , GRCh37.p13 chr1: 177,150,982-177,151,143 BRINP2
    nsv6644912copy number variation1nstd229human GRCh38 chr1: 177,179,601-177,183,200 , GRCh37.p13 chr1: 177,148,737-177,152,336 BRINP2
    nsv6331761copy number variation1nstd223human GRCh38 chr1: 177,216,568-177,216,955 , GRCh37.p13 chr1: 177,185,704-177,186,091 BRINP2
    nsv6325255copy number variation1nstd223human GRCh38 chr1: 177,243,313-177,243,774 , GRCh37.p13 chr1: 177,212,449-177,212,910 BRINP2, LOC105371625
    nsv6316445copy number variation1nstd223human GRCh38 chr1: 177,277,131-177,278,392 , GRCh37.p13 chr1: 177,246,267-177,247,528 BRINP2
    nsv6315808copy number variation1nstd223human GRCh38 chr1: 177,276,995-177,278,402 , GRCh37.p13 chr1: 177,246,131-177,247,538 BRINP2
    nsv6292542mobile element insertion1nstd186human GRCh37 chr1: 177,153,876-177,153,927 , GRCh38.p12 chr1: 177,184,740-177,184,791 BRINP2
    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
    nsv6133834copy number variation1nstd213human GRCh37 chr1: 176,040,000-177,510,001 , GRCh38.p12 chr1: 176,070,864-177,540,866 PAPPA2, COP1, 10 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