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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099208copy number variation1nstd231human GRCh38.p12 chr1: 59,526,542-66,009,490 , GRCh37 chr1: 59,992,214-66,475,173 AK4, CYP2J2, 96 more genes
    nsv7096000copy number variation1nstd102humanUncertain significance GRCh37 chr1: 63,090,910-63,902,691 , GRCh38.p12 chr1: 62,625,239-63,437,020 RPSAP65, LOC441887, 11 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7039143inversion1nstd229human GRCh38 chr1: 61,633,784-64,711,589 , GRCh37.p13 chr1: 62,099,456-65,177,272 MGC34796, RN7SL130P, 53 more genes
    nsv6653148copy number variation1nstd229human GRCh38 chr1: 63,299,706-63,321,309 , GRCh37.p13 chr1: 63,765,377-63,786,980 FOXD3-AS1, LINC00466, 1 more genes
    nsv6653050copy number variation1nstd229human GRCh38 chr1: 63,319,095-63,321,728 , GRCh37.p13 chr1: 63,784,766-63,787,399 FOXD3-AS1, FOXD3
    nsv6652904copy number variation1nstd229human GRCh38 chr1: 63,105,227-63,388,192 , GRCh37.p13 chr1: 63,570,898-63,853,863 LOC105378770, LINC00466, 7 more genes
    nsv6626042copy number variation1nstd224human GRCh37 chr1: 63,753,736-64,059,403 , GRCh38.p12 chr1: 63,288,065-63,593,732 ITGB3BP, MIR6068, 11 more genes
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6331505copy number variation1nstd223human GRCh38 chr1: 63,105,227-63,388,192 , GRCh37.p13 chr1: 63,570,898-63,853,863 ALG6, RNA5SP49, 7 more genes
    nsv5880186copy number variation1nstd209human GRCh38 chr1: 63,288,015-63,550,107 , GRCh37.p13 chr1: 63,753,686-64,015,778 LINC00466, MIR6068, 10 more genes
    nsv5830719copy number variation1nstd209human GRCh38 chr1: 63,323,950-63,326,028 , GRCh37.p13 chr1: 63,789,621-63,791,699 FOXD3, FOXD3-AS1, 1 more genes
    nsv5830111copy number variation1nstd209human GRCh38 chr1: 63,288,007-63,337,299 , GRCh37.p13 chr1: 63,753,678-63,802,970 MIR6068, FOXD3, 2 more genes
    nsv5690166mobile element insertion1nstd211human GRCh38 chr1: 63,324,876-63,324,876 , GRCh37.p13 chr1: 63,790,547-63,790,547 FOXD3-AS1, FOXD3
    nsv4903578copy number variation1nstd200human GRCh38 chr1: 63,105,226-63,388,192 , GRCh37.p13 chr1: 63,570,897-63,853,863 FOXD3, LINC00466, 7 more genes
    nsv4888344inversion1nstd200human GRCh37 chr1: 51,769,169-94,478,994 , GRCh38.p12 chr1: 51,303,497-94,013,438 , ST13P20, 664 more genes
    nsv4780904copy number variation1nstd200human GRCh37 chr1: 63,570,897-63,853,864 , GRCh38.p12 chr1: 63,105,226-63,388,193 MIR6068, LOC105378770, 7 more genes
    nsv4768338copy number variation1nstd102humanPathogenic GRCh37 chr1: 53,675,707-66,644,963 , GRCh38.p12 chr1: 53,210,035-66,179,280 TALDO1P1, LAMTOR5P1, 201 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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