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Items: 1 to 20 of 235

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076478inversion1nstd229human GRCh38 chr15: 79,261,836-81,280,491 , GRCh37.p13 chr15: 79,554,178-81,572,832 CFAP161, TMED3, 34 more genes
    nsv7069559inversion1nstd229human GRCh38 chr15: 79,698,622-80,004,412 , GRCh37.p13 chr15: 79,990,964-80,296,754 BCL2A1, ST20, 8 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv6974850copy number variation1nstd229human GRCh38 chr15: 79,877,497-79,890,346 , GRCh37.p13 chr15: 80,169,839-80,182,688 ST20-MTHFS, MTHFS
    nsv6974774copy number variation1nstd229human GRCh38 chr15: 79,246,961-80,113,369 , GRCh37.p13 chr15: 79,539,303-80,405,711 ST20-AS1, RNU6-667P, 17 more genes
    nsv6974639copy number variation1nstd229human GRCh38 chr15: 79,874,161-79,879,034 , GRCh37.p13 chr15: 80,166,503-80,171,376 MTHFS, ST20-MTHFS
    nsv6972943copy number variation1nstd229human GRCh38 chr15: 79,839,460-79,843,878 , GRCh37.p13 chr15: 80,131,802-80,136,220 MTHFS, ST20-MTHFS
    nsv6970543copy number variation1nstd229human GRCh38 chr15: 79,874,701-79,879,000 , GRCh37.p13 chr15: 80,167,043-80,171,342 MTHFS, ST20-MTHFS
    nsv6970292copy number variation1nstd229human GRCh38 chr15: 79,804,148-79,887,078 , GRCh37.p13 chr15: 80,096,490-80,179,420 MTHFS, RNU6-667P, 1 more genes
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6963736copy number variation1nstd229human GRCh38 chr15: 79,874,101-79,880,000 , GRCh37.p13 chr15: 80,166,443-80,172,342 ST20-MTHFS, MTHFS
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6637608copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,996,626-82,097,796 , GRCh38.p12 chr15: 79,704,284-81,805,455 ARNT2, LOC105370921, 31 more genes
    nsv6591397inversion1nstd223human GRCh38 chr15: 79,857,017-79,857,956 , GRCh37.p13 chr15: 80,149,359-80,150,298 MTHFS, ST20-MTHFS
    nsv6583203inversion1nstd223human GRCh38 chr15: 79,877,040-79,880,283 , GRCh37.p13 chr15: 80,169,382-80,172,625 ST20-MTHFS, MTHFS
    nsv6579530inversion1nstd223human GRCh38 chr15: 77,618,605-83,035,894 , GRCh37.p13 chr15: 77,910,947-83,704,646 CIB2, TFDP1P3, 127 more genes
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