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 1655

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965085insertion1nstd209human GRCh38 chr7: 84,099,065-84,099,065 , GRCh37.p13 chr7: 83,728,381-83,728,381 SEMA3A
    nsv5962441insertion1nstd209human GRCh38 chr7: 83,980,618-83,980,618 , GRCh37.p13 chr7: 83,609,934-83,609,934 SEMA3A
    nsv5961475insertion1nstd209human GRCh38 chr7: 84,091,120-84,091,120 , GRCh37.p13 chr7: 83,720,436-83,720,436 SEMA3A
    nsv5961397insertion1nstd209human GRCh38 chr7: 84,429,548-84,429,548 , GRCh37.p13 chr7: 84,058,864-84,058,864 SEMA3A
    nsv5958434insertion1nstd209human GRCh38 chr7: 84,056,155-84,056,155 , GRCh37.p13 chr7: 83,685,471-83,685,471 SEMA3A
    nsv5953443insertion1nstd209human GRCh38 chr7: 84,099,369-84,099,369 , GRCh37.p13 chr7: 83,728,685-83,728,685 SEMA3A
    nsv5953376insertion1nstd209human GRCh38 chr7: 84,287,037-84,287,037 , GRCh37.p13 chr7: 83,916,353-83,916,353 SEMA3A
    nsv5952132insertion1nstd209human GRCh38 chr7: 84,167,057-84,167,057 , GRCh37.p13 chr7: 83,796,373-83,796,373 SEMA3A
    nsv5947861insertion1nstd209human GRCh38 chr7: 84,445,493-84,445,493 , GRCh37.p13 chr7: 84,074,809-84,074,809 SEMA3A
    nsv5926828copy number variation1nstd209human GRCh38 chr7: 84,086,474-84,086,562 , GRCh37.p13 chr7: 83,715,790-83,715,878 SEMA3A
    nsv5925204copy number variation1nstd209human GRCh38 chr7: 84,152,304-84,157,468 , GRCh37.p13 chr7: 83,781,620-83,786,784 SEMA3A
    nsv5920548copy number variation1nstd209human GRCh38 chr7: 84,080,545-84,080,870 , GRCh37.p13 chr7: 83,709,861-83,710,186 SEMA3A
    nsv5918847copy number variation1nstd209human GRCh38 chr7: 84,255,879-84,255,937 , GRCh37.p13 chr7: 83,885,195-83,885,253 SEMA3A
    nsv5918285copy number variation1nstd209human GRCh38 chr7: 84,013,535-84,013,594 , GRCh37.p13 chr7: 83,642,851-83,642,910 SEMA3A
    nsv5917780copy number variation1nstd209human GRCh38 chr7: 84,318,307-84,318,620 , GRCh37.p13 chr7: 83,947,623-83,947,936 SEMA3A
    nsv5915491copy number variation1nstd209human GRCh38 chr7: 84,070,103-84,070,204 , GRCh37.p13 chr7: 83,699,419-83,699,520 SEMA3A
    nsv5913826copy number variation1nstd209human GRCh38 chr7: 84,287,307-84,306,388 , GRCh37.p13 chr7: 83,916,623-83,935,704 SEMA3A
    nsv5913693copy number variation1nstd209human GRCh38 chr7: 84,398,411-84,398,817 , GRCh37.p13 chr7: 84,027,727-84,028,133 SEMA3A
    nsv5912729copy number variation1nstd209human GRCh38 chr7: 84,099,074-84,099,368 , GRCh37.p13 chr7: 83,728,390-83,728,684 SEMA3A
    nsv5912532copy number variation1nstd209human GRCh38 chr7: 84,121,627-84,121,937 , GRCh37.p13 chr7: 83,750,943-83,751,253 SEMA3A
    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