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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146433insertion1nstd232human GRCh37.p13 chr2: 10,933,330-10,933,330 , GRCh38.p12 chr2: 10,793,204-10,793,204 PDIA6
    nsv7048888inversion1nstd229human GRCh38 chr2: 10,759,101-10,830,219 , GRCh37.p13 chr2: 10,899,227-10,970,345 RNU7-176P, PDIA6, 2 more genes
    nsv6676449copy number variation1nstd229human GRCh38 chr2: 10,815,527-10,828,385 , GRCh37.p13 chr2: 10,955,653-10,968,511 RNU7-176P, PDIA6
    nsv6676023copy number variation1nstd229human GRCh38 chr2: 10,775,578-10,802,181 , GRCh37.p13 chr2: 10,915,704-10,942,307 PDIA6, ATP6V1C2
    nsv6673334copy number variation1nstd229human GRCh38 chr2: 10,761,971-10,782,965 , GRCh37.p13 chr2: 10,902,097-10,923,091 LOC105373428, ATP6V1C2, 1 more genes
    nsv6672773copy number variation1nstd229human GRCh38 chr2: 10,786,040-10,835,055 , GRCh37.p13 chr2: 10,926,166-10,975,181 PDIA6, RNU7-176P
    nsv6668972copy number variation1nstd229human GRCh38 chr2: 10,687,701-10,796,400 , GRCh37.p13 chr2: 10,827,827-10,936,526 NOL10, ATP6V1C2, 4 more genes
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6664092copy number variation1nstd229human GRCh38 chr2: 10,821,763-10,823,970 , GRCh37.p13 chr2: 10,961,889-10,964,096 PDIA6
    nsv6662230copy number variation1nstd229human GRCh38 chr2: 10,782,060-10,782,113 , GRCh37.p13 chr2: 10,922,186-10,922,239 PDIA6, ATP6V1C2
    nsv6661333copy number variation1nstd229human GRCh38 chr2: 10,800,198-10,810,337 , GRCh37.p13 chr2: 10,940,324-10,950,463 PDIA6
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6353161copy number variation1nstd223human GRCh38 chr2: 10,821,763-10,823,967 , GRCh37.p13 chr2: 10,961,889-10,964,093 PDIA6
    nsv6343739copy number variation1nstd223human GRCh38 chr2: 10,791,414-10,857,108 , GRCh37.p13 chr2: 10,931,540-10,997,234 RNU7-176P, PDIA6
    nsv6341467copy number variation1nstd223human GRCh38 chr2: 10,787,063-10,788,753 , GRCh37.p13 chr2: 10,927,189-10,928,879 PDIA6
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv6242137mobile element insertion1nstd215human GRCh38 chr2: 10,806,622-10,806,622 , GRCh37.p13 chr2: 10,946,748-10,946,748 PDIA6
    nsv6167131copy number variation1nstd214human GRCh38 chr2: 10,813,740-10,813,828 , GRCh37.p13 chr2: 10,953,866-10,953,954 PDIA6, RNU7-176P
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