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 136

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6837847copy number variation1nstd229human GRCh38 chr7: 127,596,286-127,596,597 , GRCh37.p13 chr7: 127,236,340-127,236,651 FSCN3
    nsv6836828copy number variation1nstd229human GRCh38 chr7: 127,593,416-127,595,464 , GRCh37.p13 chr7: 127,233,470-127,235,518 FSCN3
    nsv6835613copy number variation1nstd229human GRCh38 chr7: 127,259,825-128,156,259 , GRCh37.p13 chr7: 126,899,879-127,796,311 LOC105375489, PRELID3BP10, 13 more genes
    nsv6820587copy number variation1nstd229human GRCh38 chr7: 127,564,125-127,689,960 , GRCh37.p13 chr7: 127,204,179-127,330,014 GCC1, FSCN3, 4 more genes
    nsv6819975copy number variation1nstd229human GRCh38 chr7: 127,596,201-127,599,100 , GRCh37.p13 chr7: 127,236,255-127,239,154 FSCN3
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6427258copy number variation1nstd223human GRCh38 chr7: 127,558,301-127,695,800 , GRCh37.p13 chr7: 127,198,355-127,335,854 PAX4, FSCN3, 4 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313722copy number variation1nstd102humanPathogenic GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221 IRF5, MIR129-1, 153 more genes
    nsv6291109copy number variation1nstd102humanUncertain significance GRCh37 chr7: 127,167,087-127,664,956 , GRCh38.p12 chr7: 127,527,033-128,024,903 LOC100196944, SND1, 7 more genes
    nsv6291032copy number variation1nstd102humanUncertain significance GRCh37 chr7: 127,050,634-127,826,231 , GRCh38.p12 chr7: 127,410,580-128,186,178 LOC100196944, SND1, 11 more genes
    nsv6265587copy number variation1nstd214human GRCh38 chr7: 127,594,185-127,594,280 , GRCh37.p13 chr7: 127,234,239-127,234,334 FSCN3
    nsv6135961copy number variation1nstd213human GRCh37 chr7: 127,140,000-129,720,001 , GRCh38.p12 chr7: 127,499,946-130,080,161 ARF5, FLNC, 74 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv6135554copy number variation1nstd213human GRCh37 chr7: 126,190,000-130,150,001 , GRCh38.p12 chr7: 126,549,946-130,510,160 IMPDH1, ODCP, 96 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center