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 167

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951702insertion1nstd209human GRCh38 chr2: 169,800,534-169,800,534 , GRCh37.p13 chr2: 170,657,044-170,657,044 SSB
    nsv5906174copy number variation1nstd209human GRCh38 chr2: 169,810,574-169,810,650 , GRCh37.p13 chr2: 170,667,084-170,667,160 SSB, METTL5
    nsv5898875copy number variation1nstd209human GRCh38 chr2: 169,796,728-169,800,268 , GRCh37.p13 chr2: 170,653,238-170,656,778 SSB
    nsv5674454mobile element insertion1nstd211human GRCh38 chr2: 169,805,897-169,805,897 , GRCh37.p13 chr2: 170,662,407-170,662,407 SSB
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5405722mobile element insertion1nstd206human GRCh38 chr2: 169,805,897-169,805,948 , GRCh37.p13 chr2: 170,662,407-170,662,458 SSB
    nsv5284830copy number variation1nstd204human GRCh37.p13 chr2: 170,658,321-170,683,509 , GRCh38.p13 chr2: 169,801,811-169,826,999 SSB, METTL5, 2 more genes
    nsv5216785copy number variation1nstd204human GRCh38.p13 chr2: 169,809,772-169,810,949 , GRCh37.p13 chr2: 170,666,282-170,667,459 SSB, METTL5
    nsv5214001copy number variation1nstd204human GRCh38.p13 chr2: 169,801,501-169,827,100 , GRCh37.p13 chr2: 170,658,011-170,683,610 METTL5, UBR3, 2 more genes
    nsv5208638copy number variation1nstd204human GRCh38.p13 chr2: 169,812,348-169,814,843 , GRCh37.p13 chr2: 170,668,858-170,671,353 SNORD3K, SSB, 1 more genes
    nsv5205128copy number variation1nstd204human GRCh38.p13 chr2: 169,801,299-169,827,078 , GRCh37.p13 chr2: 170,657,809-170,683,588 METTL5, SSB, 2 more genes
    nsv5062284mobile element insertion1nstd203human GRCh38 chr2: 169,800,534-169,800,553 , GRCh37.p13 chr2: 170,657,044-170,657,063 SSB
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4926442copy number variation1nstd200human GRCh38 chr2: 169,801,620-169,801,882 , GRCh37.p13 chr2: 170,658,130-170,658,392 SSB
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4789871copy number variation1nstd200human GRCh37 chr2: 170,653,281-170,656,781 , GRCh38.p12 chr2: 169,796,771-169,800,271 SSB
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4680847copy number variation1nstd189human GRCh37.p13 chr2: 170,339,628-170,858,121 , GRCh38.p12 chr2: 169,483,118-170,001,611 SSB, PPIG, 14 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