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Items: 1 to 20 of 751

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7142806copy number variation1nstd232human GRCh37.p13 chr20: 17,448,707-17,448,758 , GRCh38.p12 chr20: 17,468,062-17,468,113 PCSK2
    nsv7095545copy number variation1nstd102humanUncertain significance GRCh37 chr20: 17,462,209-17,511,974 , GRCh38.p12 chr20: 17,481,564-17,531,329 BFSP1, PCSK2, 1 more genes
    nsv7077806inversion1nstd229human GRCh38 chr20: 17,245,472-17,251,109 , GRCh37.p13 chr20: 17,226,117-17,231,754 PCSK2, LOC105372546
    nsv7074956inversion1nstd229human GRCh38 chr20: 17,284,938-17,284,969 , GRCh37.p13 chr20: 17,265,583-17,265,614 PCSK2, LOC105372546
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7070696inversion1nstd229human GRCh38 chr20: 17,229,500-17,237,555 , GRCh37.p13 chr20: 17,210,145-17,218,200 LOC105372546, PCSK2
    nsv7070199inversion1nstd229human GRCh38 chr20: 13,206,278-18,470,226 , GRCh37.p13 chr20: 13,186,925-18,450,870 LOC105372545, MACROD2, 73 more genes
    nsv7068244inversion1nstd229human GRCh38 chr20: 17,080,202-18,490,897 , GRCh37.p13 chr20: 17,060,847-18,471,541 DSTN, RNU2-56P, 42 more genes
    nsv7066612inversion1nstd229human GRCh38 chr20: 17,244,118-17,251,310 , GRCh37.p13 chr20: 17,224,763-17,231,955 LOC105372546, PCSK2
    nsv7065399inversion1nstd229human GRCh38 chr20: 13,871,578-20,212,622 , GRCh37.p13 chr20: 13,852,224-20,193,266 SLC24A3, LOC107985418, 92 more genes
    nsv7061810inversion1nstd229human GRCh38 chr20: 17,216,585-17,237,173 , GRCh37.p13 chr20: 17,197,230-17,217,818 LOC105372545, LOC105372546, 1 more genes
    nsv7058946inversion1nstd229human GRCh38 chr20: 17,393,554-17,397,202 , GRCh37.p13 chr20: 17,374,199-17,377,847 PCSK2
    nsv7037874copy number variation1nstd229human GRCh38 chr20: 17,320,116-17,324,071 , GRCh37.p13 chr20: 17,300,761-17,304,716 LOC105372546, PCSK2
    nsv7037010copy number variation1nstd229human GRCh38 chr20: 17,276,001-17,280,900 , GRCh37.p13 chr20: 17,256,646-17,261,545 LOC105372546, PCSK2
    nsv7036426copy number variation1nstd229human GRCh38 chr20: 16,704,017-17,308,202 , GRCh37.p13 chr20: 16,684,662-17,288,847 LOC105372546, LOC105372544, 6 more genes
    nsv7036244copy number variation1nstd229human GRCh38 chr20: 17,416,575-17,417,048 , GRCh37.p13 chr20: 17,397,220-17,397,693 PCSK2
    nsv7035902copy number variation1nstd229human GRCh38 chr20: 17,305,243-17,310,915 , GRCh37.p13 chr20: 17,285,888-17,291,560 LOC105372546, PCSK2
    nsv7035309copy number variation1nstd229human GRCh38 chr20: 17,269,429-17,269,786 , GRCh37.p13 chr20: 17,250,074-17,250,431 LOC105372546, PCSK2
    nsv7035088copy number variation1nstd229human GRCh38 chr20: 17,482,503-17,596,587 , GRCh37.p13 chr20: 17,463,148-17,577,232 BFSP1, RN7SKP69, 3 more genes
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