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Items: 1 to 20 of 682

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143173copy number variation1nstd232human GRCh37.p13 chr7: 104,590,132-104,590,235 , GRCh38.p12 chr7: 104,949,685-104,949,788 KMT2E
    nsv7097853copy number variation1nstd102humanPathogenic GRCh37 chr7: 104,456,677-108,155,935 , GRCh38.p12 chr7: 104,816,230-108,515,491 RNU6-1322P, COG5, 57 more genes
    nsv7097099copy number variation1nstd102humanUncertain significance GRCh37 chr7: 102,937,907-107,643,330 , GRCh38.p12 chr7: 103,297,460-108,002,885 SRPK2, SYPL1, 60 more genes
    nsv7057084inversion1nstd229human GRCh38 chr7: 104,984,738-104,984,826 , GRCh37.p13 chr7: 104,625,185-104,625,273 LINC01004, KMT2E
    nsv7053598inversion1nstd229human GRCh38 chr7: 104,929,020-104,966,812 , GRCh37.p13 chr7: 104,569,467-104,607,259 KMT2E
    nsv6837129copy number variation1nstd229human GRCh38 chr7: 105,086,894-105,563,170 , GRCh37.p13 chr7: 104,727,341-105,203,617 RINT1, KMT2E, 7 more genes
    nsv6836791copy number variation1nstd229human GRCh38 chr7: 105,108,958-105,109,142 , GRCh37.p13 chr7: 104,749,405-104,749,589 KMT2E, SRPK2
    nsv6836377copy number variation1nstd229human GRCh38 chr7: 105,026,795-105,035,117 , GRCh37.p13 chr7: 104,667,242-104,675,564 KMT2E
    nsv6836295copy number variation1nstd229human GRCh38 chr7: 104,924,966-104,946,069 , GRCh37.p13 chr7: 104,565,413-104,586,516 KMT2E, LHFPL3-AS2
    nsv6836084copy number variation1nstd229human GRCh38 chr7: 105,104,519-105,280,110 , GRCh37.p13 chr7: 104,744,966-104,920,557 KMT2E, SRPK2, 1 more genes
    nsv6836069copy number variation1nstd229human GRCh38 chr7: 104,937,452-104,940,790 , GRCh37.p13 chr7: 104,577,899-104,581,237 KMT2E
    nsv6835312copy number variation1nstd229human GRCh38 chr7: 104,974,751-104,975,087 , GRCh37.p13 chr7: 104,615,198-104,615,534 KMT2E
    nsv6834088copy number variation1nstd229human GRCh38 chr7: 105,069,117-105,072,016 , GRCh37.p13 chr7: 104,709,564-104,712,463 KMT2E
    nsv6833923copy number variation1nstd229human GRCh38 chr7: 104,992,428-105,081,785 , GRCh37.p13 chr7: 104,632,875-104,722,232 KMT2E, KMT2E-AS1
    nsv6833831copy number variation1nstd229human GRCh38 chr7: 105,041,301-105,060,900 , GRCh37.p13 chr7: 104,681,748-104,701,347 KMT2E
    nsv6833175copy number variation1nstd229human GRCh38 chr7: 104,942,356-104,942,756 , GRCh37.p13 chr7: 104,582,803-104,583,203 KMT2E
    nsv6832348copy number variation1nstd229human GRCh38 chr7: 105,000,793-105,004,300 , GRCh37.p13 chr7: 104,641,240-104,644,747 KMT2E
    nsv6831526copy number variation1nstd229human GRCh38 chr7: 105,095,258-105,095,809 , GRCh37.p13 chr7: 104,735,705-104,736,256 KMT2E
    nsv6831276copy number variation1nstd229human GRCh38 chr7: 105,021,297-105,022,280 , GRCh37.p13 chr7: 104,661,744-104,662,727 KMT2E
    nsv6830101copy number variation1nstd229human GRCh38 chr7: 104,949,685-104,949,789 , GRCh37.p13 chr7: 104,590,132-104,590,236 KMT2E
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