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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6911458copy number variation1nstd229human GRCh38 chr11: 77,594,199-77,656,355 , GRCh37.p13 chr11: 77,305,244-77,367,400 LOC107984369, AQP11, 1 more genes
    nsv6904714copy number variation1nstd229human GRCh38 chr11: 77,569,709-77,724,648 , GRCh37.p13 chr11: 77,280,754-77,435,693 CLNS1A, LINC03030, 3 more genes
    nsv6637911copy number variation1nstd102humanUncertain significance GRCh37 chr11: 77,211,136-78,014,355 , GRCh38.p12 chr11: 77,500,091-78,303,309 RPS20P27, RNU7-59P, 22 more genes
    nsv6595027inversion1nstd223human GRCh38 chr11: 77,626,457-77,626,792 , GRCh37.p13 chr11: 77,337,502-77,337,837 CLNS1A
    nsv6578433inversion1nstd223human GRCh38 chr11: 77,627,199-77,628,013 , GRCh37.p13 chr11: 77,338,244-77,339,058 CLNS1A
    nsv6464386copy number variation1nstd223human GRCh38 chr11: 77,569,795-77,724,740 , GRCh37.p13 chr11: 77,280,840-77,435,785 LINC03030, CLNS1A, 3 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6132116copy number variation1nstd213human GRCh37 chr11: 77,290,000-77,430,001 , GRCh38.p12 chr11: 77,578,955-77,718,956 CLNS1A, RSF1, 2 more genes
    nsv6030791copy number variation1nstd212human GRCh38 chr11: 77,627,865-77,628,080 , GRCh37.p13 chr11: 77,338,910-77,339,125 CLNS1A
    nsv5511984copy number variation1nstd206human GRCh38 chr11: 77,616,629-77,617,379 , GRCh37.p13 chr11: 77,327,674-77,328,424 CLNS1A
    nsv5499491copy number variation1nstd206human GRCh38 chr11: 77,610,772-77,624,611 , GRCh37.p13 chr11: 77,321,817-77,335,656 CLNS1A, AQP11
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5215805mobile element deletion1nstd204human GRCh38.p13 chr11: 77,626,672-77,627,021 , GRCh37.p13 chr11: 77,337,717-77,338,066 CLNS1A
    nsv4989062copy number variation1nstd200human GRCh38 chr11: 77,569,709-77,724,648 , GRCh37.p13 chr11: 77,280,754-77,435,693 AQP11, CLNS1A, 3 more genes
    nsv4987420copy number variation1nstd200human GRCh38 chr11: 77,632,143-77,632,683 , GRCh37.p13 chr11: 77,343,188-77,343,728 CLNS1A
    nsv4987419copy number variation1nstd200human GRCh38 chr11: 77,627,869-77,628,080 , GRCh37.p13 chr11: 77,338,914-77,339,125 CLNS1A
    nsv4987418copy number variation1nstd200human GRCh38 chr11: 77,626,802-77,631,840 , GRCh37.p13 chr11: 77,337,847-77,342,885 CLNS1A
    nsv4899699mobile element deletion1nstd200human GRCh38 chr11: 77,626,701-77,626,993 , GRCh37.p13 chr11: 77,337,746-77,338,038 CLNS1A
    nsv4838408copy number variation1nstd200human GRCh37 chr11: 77,280,754-77,435,693 , GRCh38.p12 chr11: 77,569,709-77,724,648 LINC03030, CLNS1A, 3 more genes
    nsv4774956mobile element deletion1nstd200human GRCh37 chr11: 77,337,746-77,338,038 , GRCh38.p12 chr11: 77,626,701-77,626,993 CLNS1A
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