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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5392636copy number variation1nstd186human GRCh37 chr12: 11,232,794-11,275,658 , GRCh38.p12 chr12: 11,080,195-11,123,059 , GRCh38.p12 chr12|NT_187658.1: 281,297-318,079 , GRCh38.p12 chr12|NW_003571050.1: 289,843-353,717 PRH1, TAS2R43, 4 more genes
    nsv4749224copy number variation1nstd199human GRCh38.p12 chr12: 11,055,075-11,125,815 , GRCh37 chr12: 11,207,674-11,278,414 , GRCh38.p12 chr12|NW_003571050.1: 253,781-356,469 , GRCh38.p12 chr12|NT_187658.1: 254,071-320,836 PRH1, TAS2R43, 6 more genes
    nsv4672636copy number variation2nstd186human GRCh37 chr12: 11,217,351-11,282,957 , GRCh38.p12 chr12: 11,064,752-11,130,358 , GRCh38.p12 chr12|NT_187658.1: 265,616-325,388 , GRCh38.p12 chr12|NW_003571050.1: 263,458-361,012 PRH1, TAS2R43, 5 more genes
    nsv4653788copy number variation3nstd186human GRCh37 chr12: 11,239,500-11,251,000 , GRCh38.p12 chr12: 11,086,901-11,098,401 , GRCh38.p12 chr12|NT_187658.1: 287,671-293,716 , GRCh38.p12 chr12|NW_003571050.1: 289,843-329,354 PRH1, TAS2R43, 4 more genes
    nsv4613365copy number variation1nstd183human GRCh37 chr12: 11,161,324-11,275,786 , GRCh38.p12 chr12|NT_187658.1: 207,420-318,207 , GRCh38.p12 chr12|NW_003571050.1: 207,431-353,845 , GRCh38.p12 chr12: 11,008,725-11,123,187 TAS2R64P, TAS2R63P, 9 more genes
    nsv4611568copy number variation2nstd183human GRCh37 chr12: 11,217,351-11,282,957 , GRCh38.p12 chr12: 11,064,752-11,130,358 , GRCh38.p12 chr12|NT_187658.1: 265,616-325,388 , GRCh38.p12 chr12|NW_003571050.1: 263,458-361,012 PRH1, TAS2R43, 5 more genes
    nsv4601539copy number variation1nstd183human GRCh37 chr12: 11,060,990-11,504,091 , GRCh38.p12 chr12|NT_187658.1: 107,097-546,120 , GRCh38.p12 chr12|NW_003571050.1: 107,097-408,271 , GRCh38.p12 chr12: 10,908,391-11,351,157 , TAS2R64P, 26 more genes
    nsv4430681copy number variation1nstd174human GRCh37 chr12: 11,210,023-11,328,131 , GRCh38.p12 chr12: 11,057,424-11,175,532 , GRCh38.p12 chr12|NT_187658.1: 258,288-370,471 , GRCh38.p12 chr12|NW_003571050.1: 256,130-406,186 TAS2R68P, TAS2R45, 9 more genes
    nsv4429390copy number variation1nstd174human GRCh37 chr12: 11,161,281-11,293,747 , GRCh38.p12 chr12|NW_003571050.1: 207,388-371,802 , GRCh38.p12 chr12: 11,008,682-11,141,148 , GRCh38.p12 chr12|NT_187658.1: 207,377-336,130 TAS2R31, PRH1-TAS2R14, 10 more genes
    nsv4428906copy number variation1nstd174human GRCh37 chr12: 11,228,874-11,290,245 , GRCh38.p12 chr12: 11,076,275-11,137,646 , GRCh38.p12 chr12|NT_187658.1: 277,341-332,626 , GRCh38.p12 chr12|NW_003571050.1: 289,843-368,300 PRH1, TAS2R43, 6 more genes
    nsv4423965copy number variation1nstd174human GRCh37 chr12: 11,179,034-11,256,817 , GRCh38.p12 chr12|NT_187658.1: 225,440-299,538 , GRCh38.p12 chr12: 11,026,435-11,104,218 , GRCh38.p12 chr12|NW_003571050.1: 225,141-335,176 PRH1-TAS2R14, TAS2R46, 8 more genes
    nsv4415265copy number variation1nstd174human GRCh37 chr12: 11,210,529-11,257,329 , GRCh38.p12 chr12: 11,057,930-11,104,730 , GRCh38.p12 chr12|NT_187658.1: 258,794-300,054 , GRCh38.p12 chr12|NW_003571050.1: 256,636-335,692 PRH1, TAS2R43, 6 more genes
    nsv4414885copy number variation1nstd174human GRCh37 chr12: 11,204,143-11,280,303 , GRCh38.p12 chr12: 11,051,544-11,127,704 , GRCh38.p12 chr12|NT_187658.1: 250,544-322,725 , GRCh38.p12 chr12|NW_003571050.1: 250,250-358,358 PRH1, TAS2R43, 6 more genes
    nsv4374889copy number variation1nstd173human GRCh37 chr12: 11,208,695-11,256,817 , GRCh38.p12 chr12: 11,056,096-11,104,218 , GRCh38.p12 chr12|NT_187658.1: 256,962-299,538 , GRCh38.p12 chr12|NW_003571050.1: 254,802-335,176 TAS2R45, PRH1-PRR4, 6 more genes
    nsv4194930copy number variation1nstd166human GRCh37.p13 chr12: 11,170,675-11,283,000 , GRCh38.p12 chr12|NW_003571050.1: 216,782-361,055 , GRCh38.p12 chr12|NT_187658.1: 216,775-325,431 , GRCh38.p12 chr12: 11,018,076-11,130,401 PRH1-PRR4, PRH1, 9 more genes
    nsv4037105copy number variation3nstd166human GRCh37.p13 chr12: 11,239,500-11,251,000 , GRCh38.p12 chr12: 11,086,901-11,098,401 , GRCh38.p12 chr12|NT_187658.1: 287,671-293,716 , GRCh38.p12 chr12|NW_003571050.1: 289,843-329,354 PRH1, TAS2R43, 4 more genes
    nsv3908446copy number variation1nstd102humanBenign GRCh37 chr12: 11,174,276-11,272,192 , GRCh38.p12 chr12|NT_187658.1: 220,371-314,617 , GRCh38.p12 chr12: 11,021,677-11,119,593 , GRCh38.p12 chr12|NW_003571050.1: 220,383-350,255 TAS2R68P, TAS2R43, 9 more genes
    nsv3899764copy number variation1nstd102humanUncertain significance GRCh37 chr12: 11,047,687-11,751,920 , GRCh38.p12 chr12: 10,895,088-11,598,986 , GRCh38.p12 chr12|NT_187658.1: 93,794-572,349 HIGD1AP8, PRB2, 33 more genes
    nsv3898175copy number variation1nstd102humanLikely benign GRCh37 chr12: 11,043,965-11,260,347 , GRCh38.p12 chr12|NT_187658.1: 90,072-302,777 , GRCh38.p12 chr12|NW_003571050.1: 90,072-338,415 , GRCh38.p12 chr12: 10,891,366-11,107,748 PRH2, TAS2R12P, 16 more genes
    nsv3891206copy number variation1nstd102humanBenign GRCh37 chr12: 11,188,140-11,252,845 , GRCh38.p12 chr12: 11,035,541-11,100,246 , GRCh38.p12 chr12|NT_187658.1: 234,539-295,561 , GRCh38.p12 chr12|NW_003571050.1: 234,247-331,199 PRH1, TAS2R43, 7 more genes
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