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Items: 1 to 20 of 425

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096096copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr21: 43,160,998-47,754,702 , GRCh38.p12 chr21: 41,740,838-46,334,788 TSPEAR, LINC01424, 158 more genes
    nsv7037973copy number variation1nstd229human GRCh38 chr21: 46,121,114-46,351,190 , GRCh37.p13 chr21: 47,541,028-47,771,104 C21orf58, PCNT, 9 more genes
    nsv7036756copy number variation1nstd229human GRCh38 chr21: 46,299,174-46,305,365 , GRCh37.p13 chr21: 47,719,088-47,725,279 YBEY, C21orf58
    nsv7034560copy number variation1nstd229human GRCh38 chr21: 46,304,393-46,306,372 , GRCh37.p13 chr21: 47,724,307-47,726,286 YBEY, C21orf58
    nsv7034392copy number variation1nstd229human GRCh38 chr21: 46,318,764-46,319,896 , GRCh37.p13 chr21: 47,738,678-47,739,810 C21orf58
    nsv7033879copy number variation1nstd229human GRCh38 chr21: 46,314,901-46,339,100 , GRCh37.p13 chr21: 47,734,815-47,759,014 C21orf58, PCNT
    nsv7033390copy number variation1nstd229human GRCh38 chr21: 46,324,534-46,332,526 , GRCh37.p13 chr21: 47,744,448-47,752,440 C21orf58, PCNT
    nsv7033089copy number variation1nstd229human GRCh38 chr21: 46,228,625-46,331,082 , GRCh37.p13 chr21: 47,648,539-47,750,996 MCM3AP, LSS, 4 more genes
    nsv7031848copy number variation1nstd229human GRCh38 chr21: 46,308,393-46,312,106 , GRCh37.p13 chr21: 47,728,307-47,732,020 YBEY, C21orf58
    nsv7029910copy number variation1nstd229human GRCh38 chr21: 46,015,310-46,317,714 , GRCh37.p13 chr21: 47,435,224-47,737,628 MCM3AP, C21orf58, 10 more genes
    nsv7029880copy number variation1nstd229human GRCh38 chr21: 46,290,037-46,304,189 , GRCh37.p13 chr21: 47,709,951-47,724,103 YBEY, C21orf58
    nsv7029586copy number variation1nstd229human GRCh38 chr21: 46,318,464-46,320,443 , GRCh37.p13 chr21: 47,738,378-47,740,357 C21orf58
    nsv7027585copy number variation1nstd229human GRCh38 chr21: 46,321,658-46,372,796 , GRCh37.p13 chr21: 47,741,572-47,792,711 C21orf58, PCNT
    nsv7026746copy number variation1nstd229human GRCh38 chr21: 46,310,812-46,310,863 , GRCh37.p13 chr21: 47,730,726-47,730,777 YBEY, C21orf58
    nsv7022890copy number variation1nstd229human GRCh38 chr21: 46,275,382-46,366,879 , GRCh37.p13 chr21: 47,695,296-47,786,794 MCM3AP, C21orf58, 2 more genes
    nsv6637891copy number variation1nstd102humanUncertain significance GRCh37 chr21: 46,882,064-47,963,149 , GRCh38.p12 chr21: 45,462,150-46,543,236 C21orf58, PCNT, 25 more genes
    nsv6637626copy number variation1nstd102humanUncertain significance GRCh37 chr21: 47,500,415-48,097,372 , GRCh38.p12 chr21: 46,080,501-46,677,460 FTCD-AS1, PCNT, 16 more genes
    nsv6637307copy number variation1nstd102humanUncertain significance GRCh37 chr21: 47,563,980-48,097,372 , GRCh38.p12 chr21: 46,144,066-46,677,460 PCNT, DIP2A, 15 more genes
    nsv6626888copy number variation1nstd224human GRCh37 chr21: 47,699,982-47,786,950 , GRCh38.p12 chr21: 46,280,068-46,367,035 PCNT, MCM3AP, 2 more genes
    nsv6626653copy number variation1nstd224human GRCh37 chr21: 47,711,344-47,739,146 , GRCh38.p12 chr21: 46,291,430-46,319,232 YBEY, C21orf58
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