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Items: 1 to 20 of 447

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094111copy number variation1nstd102humanPathogenic GRCh37 chr11: 85,339,652-86,666,127 , GRCh38.p12 chr11: 85,628,608-86,955,085 PRSS23, OR7E13P, 30 more genes
    nsv7069436inversion1nstd229human GRCh38 chr11: 85,936,971-89,461,473 , GRCh37.p13 chr11: 85,648,014-89,194,641 , RNU6-1135P, 45 more genes
    nsv7068892inversion1nstd229human GRCh38 chr11: 85,482,651-87,653,297 , GRCh37.p13 chr11: 85,193,695-87,364,189 , RNU6-1292P, 42 more genes
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv7062125inversion1nstd229human GRCh38 chr11: 85,974,357-86,045,056 , GRCh37.p13 chr11: 85,685,400-85,756,098 PICALM
    nsv7059340inversion1nstd229human GRCh38 chr11: 85,686,066-86,073,216 , GRCh37.p13 chr11: 85,397,109-85,784,258 PICALM, CCDC89, 4 more genes
    nsv6916412copy number variation1nstd229human GRCh38 chr11: 86,050,601-86,054,000 , GRCh37.p13 chr11: 85,761,643-85,765,042 PICALM
    nsv6913551copy number variation1nstd229human GRCh38 chr11: 86,038,555-86,048,563 , GRCh37.p13 chr11: 85,749,597-85,759,605 PICALM
    nsv6913350copy number variation1nstd229human GRCh38 chr11: 86,035,083-86,064,940 , GRCh37.p13 chr11: 85,746,125-85,775,982 PICALM
    nsv6911943copy number variation1nstd229human GRCh38 chr11: 85,948,901-85,957,000 , GRCh37.p13 chr11: 85,659,944-85,668,043 PICALM
    nsv6910907copy number variation1nstd229human GRCh38 chr11: 85,984,624-85,989,115 , GRCh37.p13 chr11: 85,695,667-85,700,158 PICALM
    nsv6908309copy number variation1nstd229human GRCh38 chr11: 85,947,563-86,012,317 , GRCh37.p13 chr11: 85,658,606-85,723,360 PICALM
    nsv6905543copy number variation1nstd229human GRCh38 chr11: 84,763,504-86,648,143 , GRCh37.p13 chr11: 84,474,547-86,359,185 CCDC83, CCDC81, 25 more genes
    nsv6904836copy number variation1nstd229human GRCh38 chr11: 86,069,644-86,074,914 , GRCh37.p13 chr11: 85,780,686-85,785,956 PICALM
    nsv6903481copy number variation1nstd229human GRCh38 chr11: 86,042,148-86,049,551 , GRCh37.p13 chr11: 85,753,190-85,760,593 PICALM
    nsv6902082copy number variation1nstd229human GRCh38 chr11: 86,061,636-86,274,238 , GRCh37.p13 chr11: 85,772,678-85,985,280 LINC02695, PICALM, 3 more genes
    nsv6898992copy number variation1nstd229human GRCh38 chr11: 86,003,761-86,003,919 , GRCh37.p13 chr11: 85,714,804-85,714,962 PICALM
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6621210copy number variation1nstd224human GRCh37 chr11: 85,576,127-85,893,436 , GRCh38.p12 chr11: 85,865,084-86,182,394 PICALM, SLC25A1P1, 2 more genes
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