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Items: 1 to 20 of 683

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 ENTPD4, LOC100421446, 447 more genes
    nsv7148146copy number variation1nstd102humanPathogenic GRCh38 chr8: 12,721,809-30,183,737 , GRCh37.p13 chr8: 12,579,318-30,041,253 LOC101929028, RPL35P6, 274 more genes
    nsv7098901copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 21,925,038-26,372,195 , GRCh38.p12 chr8: 22,067,527-26,514,679 BMP1, POLR3D, 95 more genes
    nsv7074761inversion1nstd229human GRCh38 chr8: 22,699,805-23,128,957 , GRCh37.p13 chr8: 22,557,318-22,986,470 LOC105379325, LOC101929237, 10 more genes
    nsv7073429inversion1nstd229human GRCh38 chr8: 22,689,880-24,095,801 , GRCh37.p13 chr8: 22,547,393-23,953,314 TNFRSF10B, RNU1-148P, 34 more genes
    nsv7068325inversion1nstd229human GRCh38 chr8: 22,905,495-22,905,564 , GRCh37.p13 chr8: 22,763,008-22,763,077 PEBP4
    nsv7066374inversion1nstd229human GRCh38 chr8: 22,859,848-22,866,980 , GRCh37.p13 chr8: 22,717,361-22,724,493 PEBP4
    nsv7058432inversion1nstd229human GRCh38 chr8: 22,912,783-22,927,133 , GRCh37.p13 chr8: 22,770,296-22,784,646 PEBP4
    nsv6858062copy number variation1nstd229human GRCh38 chr8: 22,796,833-22,797,360 , GRCh37.p13 chr8: 22,654,346-22,654,873 PEBP4
    nsv6858041copy number variation1nstd229human GRCh38 chr8: 22,816,651-22,820,179 , GRCh37.p13 chr8: 22,674,164-22,677,692 PEBP4, LOC105379325
    nsv6857760copy number variation1nstd229human GRCh38 chr8: 22,921,299-22,925,097 , GRCh37.p13 chr8: 22,778,812-22,782,610 PEBP4
    nsv6856538copy number variation1nstd229human GRCh38 chr8: 22,819,418-22,830,361 , GRCh37.p13 chr8: 22,676,931-22,687,874 PEBP4
    nsv6856450copy number variation1nstd229human GRCh38 chr8: 22,919,504-23,266,199 , GRCh37.p13 chr8: 22,777,017-23,123,712 CHMP7, LOC254896, 11 more genes
    nsv6855350copy number variation1nstd229human GRCh38 chr8: 22,862,536-22,865,454 , GRCh37.p13 chr8: 22,720,049-22,722,967 PEBP4
    nsv6854756copy number variation1nstd229human GRCh38 chr8: 22,893,942-22,898,629 , GRCh37.p13 chr8: 22,751,455-22,756,142 PEBP4
    nsv6853870copy number variation1nstd229human GRCh38 chr8: 22,891,629-22,892,061 , GRCh37.p13 chr8: 22,749,142-22,749,574 PEBP4
    nsv6852877copy number variation1nstd229human GRCh38 chr8: 22,858,222-22,858,628 , GRCh37.p13 chr8: 22,715,735-22,716,141 PEBP4
    nsv6852778copy number variation1nstd229human GRCh38 chr8: 22,724,854-22,733,292 , GRCh37.p13 chr8: 22,582,367-22,590,805 PEBP4, LOC107986925
    nsv6852401copy number variation1nstd229human GRCh38 chr8: 22,941,093-23,155,466 , GRCh37.p13 chr8: 22,798,606-23,012,979 TNFRSF10C, RHOBTB2, 7 more genes
    nsv6852177copy number variation1nstd229human GRCh38 chr8: 22,902,037-22,919,503 , GRCh37.p13 chr8: 22,759,550-22,777,016 PEBP4
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