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Items: 1 to 20 of 276

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148047copy number variation1nstd102humanUncertain significance GRCh38 chr1: 63,395,673-63,749,318 , GRCh37.p13 chr1: 63,861,344-64,214,989 LOC102724319, ITGB3BP, 8 more genes
    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
    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
    nsv7051324inversion1nstd229human GRCh38 chr1: 63,565,672-63,565,805 , GRCh37.p13 chr1: 64,031,343-64,031,476 EFCAB7
    nsv7041140inversion1nstd229human GRCh38 chr1: 63,514,069-63,623,155 , GRCh37.p13 chr1: 63,979,740-64,088,826 RNU7-123P, PGM1, 5 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
    nsv6653156copy number variation1nstd229human GRCh38 chr1: 63,534,501-63,548,100 , GRCh37.p13 chr1: 64,000,172-64,013,771 EFCAB7, DLEU2L, 1 more genes
    nsv6653155copy number variation1nstd229human GRCh38 chr1: 63,515,592-63,522,765 , GRCh37.p13 chr1: 63,981,263-63,988,436 LOC102724319, ITGB3BP, 1 more genes
    nsv6653057copy number variation1nstd229human GRCh38 chr1: 63,564,701-63,569,500 , GRCh37.p13 chr1: 64,030,372-64,035,171 EFCAB7
    nsv6653056copy number variation1nstd229human GRCh38 chr1: 63,522,176-63,524,629 , GRCh37.p13 chr1: 63,987,847-63,990,300 ITGB3BP, EFCAB7
    nsv6652923copy number variation1nstd229human GRCh38 chr1: 63,583,065-63,583,107 , GRCh37.p13 chr1: 64,048,736-64,048,778 EFCAB7
    nsv6652922copy number variation1nstd229human GRCh38 chr1: 63,543,701-63,546,800 , GRCh37.p13 chr1: 64,009,372-64,012,471 EFCAB7
    nsv6652921copy number variation1nstd229human GRCh38 chr1: 63,514,470-63,525,881 , GRCh37.p13 chr1: 63,980,141-63,991,552 ITGB3BP, EFCAB7, 1 more genes
    nsv6652920copy number variation1nstd229human GRCh38 chr1: 63,509,384-63,522,302 , GRCh37.p13 chr1: 63,975,055-63,987,973 LOC102724319, ITGB3BP, 1 more genes
    nsv6652395copy number variation1nstd229human GRCh38 chr1: 63,575,515-63,581,784 , GRCh37.p13 chr1: 64,041,186-64,047,455 EFCAB7
    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
    nsv6542032inversion1nstd223human GRCh38 chr1: 63,529,612-63,529,802 , GRCh37.p13 chr1: 63,995,283-63,995,473 ITGB3BP, EFCAB7, 1 more genes
    nsv6541303inversion1nstd223human GRCh38 chr1: 63,559,319-63,560,466 , GRCh37.p13 chr1: 64,024,990-64,026,137 EFCAB7
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