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 262

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5905685copy number variation1nstd209human GRCh38 chr4: 155,217,270-155,219,795 , GRCh37.p13 chr4: 156,138,422-156,140,947 NPY2R
    nsv5900246copy number variation1nstd209human GRCh38 chr4: 155,181,452-155,187,103 , GRCh37.p13 chr4: 156,102,604-156,108,255 NPY2R
    nsv5893811copy number variation1nstd209human GRCh38 chr4: 155,194,161-155,194,285 , GRCh37.p13 chr4: 156,115,313-156,115,437 NPY2R
    nsv5838072copy number variation2nstd209human GRCh38 chr4: 155,185,634-155,187,911 , GRCh37.p13 chr4: 156,106,786-156,109,063 NPY2R
    nsv5837765copy number variation1nstd209human GRCh38 chr4: 155,217,211-155,219,867 , GRCh37.p13 chr4: 156,138,363-156,141,019 NPY2R
    nsv5837764copy number variation1nstd209human GRCh38 chr4: 155,181,534-155,187,133 , GRCh37.p13 chr4: 156,102,686-156,108,285 NPY2R
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5556143sequence alteration1nstd206human GRCh38 chr4: 155,187,626-155,188,291 , GRCh37.p13 chr4: 156,108,778-156,109,443 NPY2R
    nsv5472328copy number variation1nstd206human GRCh38 chr4: 155,181,036-155,181,089 , GRCh37.p13 chr4: 156,102,188-156,102,241 NPY2R
    nsv5471758copy number variation1nstd206human GRCh38 chr4: 155,217,270-155,219,796 , GRCh37.p13 chr4: 156,138,422-156,140,948 NPY2R
    nsv5462909copy number variation1nstd206human GRCh38 chr4: 155,194,161-155,194,291 , GRCh37.p13 chr4: 156,115,313-156,115,443 NPY2R
    nsv5353320translocation1nstd200human GRCh38 chr4: 155,217,270-155,217,270 , GRCh38 chr4: 155,219,796-155,219,796 , GRCh37.p13 chr4: 156,138,422-156,138,422 , GRCh37.p13 chr4: 156,140,948-156,140,948 NPY2R
    nsv5331771translocation1nstd200human GRCh37 chr4: 156,138,422-156,138,422 , GRCh37 chr4: 156,140,948-156,140,948 , GRCh38.p12 chr4: 155,217,270-155,217,270 , GRCh38.p12 chr4: 155,219,796-155,219,796 NPY2R
    nsv5303339copy number variation1nstd204human GRCh38.p13 chr4: 155,217,247-155,219,825 , GRCh37.p13 chr4: 156,138,399-156,140,977 NPY2R
    nsv5235972copy number variation1nstd204human GRCh38.p13 chr4: 155,217,411-155,218,960 , GRCh37.p13 chr4: 156,138,563-156,140,112 NPY2R
    nsv5227434copy number variation1nstd204human GRCh38.p13 chr4: 155,217,301-155,219,800 , GRCh37.p13 chr4: 156,138,453-156,140,952 NPY2R
    nsv5082266mobile element insertion1nstd203human GRCh38 chr4: 155,205,965-155,205,979 , GRCh37.p13 chr4: 156,127,117-156,127,131 NPY2R-AS1, NPY2R
    nsv4929787copy number variation1nstd200human GRCh38 chr4: 155,190,824-155,191,567 , GRCh37.p13 chr4: 156,111,976-156,112,719 NPY2R
    nsv4929786copy number variation1nstd200human GRCh38 chr4: 155,189,430-155,190,747 , GRCh37.p13 chr4: 156,110,582-156,111,899 NPY2R
    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