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 777

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131150insertion1nstd186human GRCh37 chr18: 31,571,945-31,571,993 , GRCh38.p12 chr18: 33,991,981-33,992,029 NOL4
    nsv6130056insertion1nstd186human GRCh37 chr18: 31,563,384-31,563,429 , GRCh38.p12 chr18: 33,983,420-33,983,465 NOL4
    nsv6112851mobile element insertion1nstd186human GRCh37 chr18: 31,533,191-31,533,191 , GRCh38.p12 chr18: 33,953,227-33,953,227 NOL4
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5979860inversion1nstd209human GRCh38 chr18: 33,885,441-33,886,792 , GRCh37.p13 chr18: 31,465,405-31,466,756 NOL4
    nsv5976670insertion1nstd209human GRCh38 chr18: 33,953,470-33,953,470 , GRCh37.p13 chr18: 31,533,434-31,533,434 NOL4
    nsv5975750insertion1nstd209human GRCh38 chr18: 33,953,227-33,953,227 , GRCh37.p13 chr18: 31,533,191-31,533,191 NOL4
    nsv5974614insertion1nstd209human GRCh38 chr18: 33,991,978-33,991,978 , GRCh37.p13 chr18: 31,571,942-31,571,942 NOL4
    nsv5947338copy number variation1nstd209human GRCh38 chr18: 34,119,778-34,121,612 , GRCh37.p13 chr18: 31,699,742-31,701,576 NOL4
    nsv5930473copy number variation1nstd209human GRCh38 chr18: 33,975,865-34,014,368 , GRCh37.p13 chr18: 31,555,829-31,594,332 NOL4
    nsv5930308copy number variation1nstd209human GRCh38 chr18: 34,115,091-34,115,167 , GRCh37.p13 chr18: 31,695,055-31,695,131 NOL4
    nsv5929383copy number variation1nstd209human GRCh38 chr18: 34,166,741-34,167,077 , GRCh37.p13 chr18: 31,746,705-31,747,041 NOL4
    nsv5927999copy number variation1nstd209human GRCh38 chr18: 34,145,392-34,146,327 , GRCh37.p13 chr18: 31,725,356-31,726,291 NOL4
    nsv5882209copy number variation2nstd209human GRCh38 chr18: 34,005,735-34,006,834 , GRCh37.p13 chr18: 31,585,699-31,586,798 NOL4
    nsv5880401copy number variation1nstd209human GRCh38 chr18: 34,119,799-34,121,448 , GRCh37.p13 chr18: 31,699,763-31,701,412 NOL4
    nsv5878357copy number variation1nstd209human GRCh38 chr18: 33,975,807-34,007,934 , GRCh37.p13 chr18: 31,555,771-31,587,898 NOL4
    nsv5729008mobile element insertion1nstd211human GRCh38 chr18: 33,915,624-33,915,624 , GRCh37.p13 chr18: 31,495,588-31,495,588 NOL4
    nsv5708507mobile element insertion1nstd211human GRCh38 chr18: 34,189,066-34,189,066 , GRCh37.p13 chr18: 31,769,030-31,769,030 NOL4
    nsv5706238mobile element insertion1nstd211human GRCh38 chr18: 34,003,067-34,003,067 , GRCh37.p13 chr18: 31,583,031-31,583,031 NOL4
    nsv5704324mobile element insertion2nstd211human GRCh38 chr18: 34,167,080-34,167,080 , GRCh37.p13 chr18: 31,747,044-31,747,044 NOL4
    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