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 186

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964579insertion1nstd209human GRCh38 chr1: 220,781,003-220,781,003 , GRCh37.p13 chr1: 220,954,345-220,954,345 MTARC2
    nsv5682175mobile element insertion2nstd211human GRCh38 chr1: 220,781,017-220,781,017 , GRCh37.p13 chr1: 220,954,359-220,954,359 MTARC2
    nsv5621133insertion1nstd207human GRCh38 chr1: 220,781,003-220,781,003 , GRCh37.p13 chr1: 220,954,345-220,954,345 MTARC2
    nsv5443213copy number variation1nstd206human GRCh38 chr1: 220,780,545-220,780,990 , GRCh37.p13 chr1: 220,953,887-220,954,332 MTARC2
    nsv5413844mobile element insertion1nstd206human GRCh38 chr1: 220,781,017-220,781,068 , GRCh37.p13 chr1: 220,954,359-220,954,410 MTARC2
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5076961mobile element insertion1nstd203human GRCh38 chr1: 220,781,003-220,781,017 , GRCh37.p13 chr1: 220,954,345-220,954,359 MTARC2
    nsv5075216mobile element insertion1nstd203human GRCh38 chr1: 220,781,007-220,781,017 , GRCh37.p13 chr1: 220,954,349-220,954,359 MTARC2
    nsv5072471mobile element insertion1nstd203human GRCh38 chr1: 220,772,867-220,772,883 , GRCh37.p13 chr1: 220,946,209-220,946,225 MTARC2
    nsv5070519mobile element insertion1nstd203human GRCh38 chr1: 220,781,002-220,781,017 , GRCh37.p13 chr1: 220,954,344-220,954,359 MTARC2
    nsv5069939mobile element insertion1nstd203human GRCh38 chr1: 220,781,009-220,781,017 , GRCh37.p13 chr1: 220,954,351-220,954,359 MTARC2
    nsv5066782mobile element insertion1nstd203human GRCh38 chr1: 220,781,008-220,781,017 , GRCh37.p13 chr1: 220,954,350-220,954,359 MTARC2
    nsv4898843copy number variation1nstd200human GRCh38 chr1: 220,757,048-220,758,492 , GRCh37.p13 chr1: 220,930,390-220,931,834 MTARC2
    nsv4898842copy number variation1nstd200human GRCh38 chr1: 220,752,088-220,783,137 , GRCh37.p13 chr1: 220,925,430-220,956,479 MTARC2
    nsv4898841copy number variation1nstd200human GRCh38 chr1: 220,745,950-220,749,678 , GRCh37.p13 chr1: 220,919,292-220,923,020 MTARC2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4760247insertion1nstd199human GRCh37 chr1: 220,954,351-220,954,351 , GRCh38.p12 chr1: 220,781,009-220,781,009 MTARC2
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4691627mobile element insertion1nstd186human GRCh37 chr1: 220,954,371-220,954,371 , GRCh38.p12 chr1: 220,781,029-220,781,029 MTARC2
    nsv4684187copy number variation1nstd102humanPathogenic GRCh37 chr1: 210,152,794-249,218,992 , GRCh38.p12 chr1: 209,979,449-248,924,793 HLX-AS1, OPN3, 740 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