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 141

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5878025copy number variation1nstd209human GRCh38 chr1: 12,017,159-12,017,781 , GRCh37.p13 chr1: 12,077,216-12,077,838 MIIP
    nsv5430888copy number variation1nstd206human GRCh38 chr1: 12,017,096-12,025,879 , GRCh37.p13 chr1: 12,077,153-12,085,936 MIIP
    nsv5427165copy number variation1nstd206human GRCh38 chr1: 12,017,194-12,018,058 , GRCh37.p13 chr1: 12,077,251-12,078,115 MIIP
    nsv5295459copy number variation1nstd204human GRCh38.p13 chr1: 12,024,165-12,026,270 , GRCh37.p13 chr1: 12,084,222-12,086,327 MIIP
    nsv5295281copy number variation1nstd204human GRCh38.p13 chr1: 11,808,402-12,053,478 , GRCh37.p13 chr1: 11,868,459-12,113,535 RNU5E-1, RN7SL649P, 11 more genes
    nsv5216876copy number variation1nstd204human GRCh38.p13 chr1: 12,028,610-12,049,029 , GRCh37.p13 chr1: 12,088,667-12,109,086 MIR6729, RN7SL649P, 1 more genes
    nsv5210869copy number variation1nstd204human GRCh38.p13 chr1: 11,808,401-12,053,900 , GRCh37.p13 chr1: 11,868,458-12,113,957 NPPB, KIAA2013, 11 more genes
    nsv5079526mobile element insertion1nstd203human GRCh38 chr1: 12,018,103-12,018,103 , GRCh37.p13 chr1: 12,078,160-12,078,160 MIIP
    nsv5076377mobile element insertion1nstd203human GRCh38 chr1: 12,018,937-12,018,959 , GRCh37.p13 chr1: 12,078,994-12,079,016 MIIP
    nsv5060962mobile element insertion1nstd203human GRCh38 chr1: 12,018,948-12,018,957 , GRCh37.p13 chr1: 12,079,005-12,079,014 MIIP
    nsv4903069copy number variation1nstd200human GRCh38 chr1: 11,808,412-12,053,469 , GRCh37.p13 chr1: 11,868,469-12,113,526 NPPB, MIIP, 11 more genes
    nsv4889922copy number variation1nstd200human GRCh38 chr1: 12,023,626-12,030,206 , GRCh37.p13 chr1: 12,083,683-12,090,263 MIR6729, MIIP
    nsv4889921copy number variation1nstd200human GRCh38 chr1: 12,020,793-12,020,886 , GRCh37.p13 chr1: 12,080,850-12,080,943 MIIP
    nsv4782996copy number variation1nstd200human GRCh37 chr1: 12,083,683-12,090,263 , GRCh38.p12 chr1: 12,023,626-12,030,206 MIIP, MIR6729
    nsv4782995copy number variation1nstd200human GRCh37 chr1: 12,080,850-12,080,943 , GRCh38.p12 chr1: 12,020,793-12,020,886 MIIP
    nsv4782994copy number variation1nstd200human GRCh37 chr1: 12,077,250-12,077,849 , GRCh38.p12 chr1: 12,017,193-12,017,792 MIIP
    nsv4772165copy number variation1nstd200human GRCh37 chr1: 11,868,469-12,113,526 , GRCh38.p12 chr1: 11,808,412-12,053,469 RN7SL649P, RNU5E-1, 11 more genes
    nsv4517605copy number variation1nstd166human GRCh37.p13 chr1: 12,064,000-12,141,000 , GRCh38.p12 chr1: 12,003,943-12,080,943 TNFRSF8, MFN2, 5 more genes
    nsv4454705copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,246,640-12,841,900 , GRCh38.p12 chr1: 10,186,582-12,781,757 LINC01647, MIR7846, 73 more genes
    nsv4436711copy number variation1nstd102humanPathogenic GRCh37 chr1: 11,794,553-12,786,444 , GRCh38.p12 chr1: 11,734,496-12,726,477 MIR4632, AADACL3, 31 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