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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094180copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,761,127-67,761,285 , GRCh38.p12 chr11: 67,993,656-67,993,814 UNC93B1
    nsv7094099copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,759,017-68,216,538 , GRCh38.p12 chr11: 67,991,546-68,449,070 LRP5, UNC93B1, 11 more genes
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7075540inversion1nstd229human GRCh38 chr11: 67,968,443-71,626,784 , GRCh37.p13 chr11: 67,735,914-71,337,830 S100A11P3, CCND1, 76 more genes
    nsv7063416inversion1nstd229human GRCh38 chr11: 67,577,505-68,052,740 , GRCh37.p13 chr11: 67,344,976-67,820,207 ALDH3B1, FAM86C2P, 30 more genes
    nsv6912757copy number variation1nstd229human GRCh38 chr11: 66,793,001-68,121,500 , GRCh37.p13 chr11: 66,560,472-67,888,967 CHKA-DT, LOC107984341, 66 more genes
    nsv6911763copy number variation1nstd229human GRCh38 chr11: 67,577,408-68,033,450 , GRCh37.p13 chr11: 67,344,879-67,800,917 LINC02754, LOC112268076, 27 more genes
    nsv6911508copy number variation1nstd229human GRCh38 chr11: 67,541,590-68,051,961 , GRCh37.p13 chr11: 67,309,061-67,819,428 NDUFV1, ENPP7P7, 30 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6905813copy number variation1nstd229human GRCh38 chr11: 67,694,101-68,081,300 , GRCh37.p13 chr11: 67,461,572-67,848,767 OR7E1P, UNC93B5, 21 more genes
    nsv6905481copy number variation1nstd229human GRCh38 chr11: 68,001,201-68,010,600 , GRCh37.p13 chr11: 67,768,671-67,778,070 UNC93B1, ALDH3B1
    nsv6905360copy number variation1nstd229human GRCh38 chr11: 67,712,738-67,992,929 , GRCh37.p13 chr11: 67,480,209-67,760,400 ALG1L8P, LOC112268076, 14 more genes
    nsv6903563copy number variation1nstd229human GRCh38 chr11: 67,709,965-67,990,025 , GRCh37.p13 chr11: 67,477,436-67,757,496 UNC93B1, ALG1L8P, 14 more genes
    nsv6901523copy number variation1nstd229human GRCh38 chr11: 67,577,616-67,989,511 , GRCh37.p13 chr11: 67,345,087-67,756,982 EVA1CP4, LINC02754, 23 more genes
    nsv6898933copy number variation1nstd229human GRCh38 chr11: 67,713,018-67,994,849 , GRCh37.p13 chr11: 67,480,489-67,762,320 EVA1CP4, LINC02754, 14 more genes
    nsv6621017copy number variation1nstd224human GRCh37 chr11: 67,501,626-67,767,052 , GRCh38.p12 chr11: 67,734,155-67,999,582 LOC105369359, UNC93B1, 12 more genes
    nsv6459128copy number variation1nstd223human GRCh38 chr11: 67,577,616-67,989,511 , GRCh37.p13 chr11: 67,345,087-67,756,982 OR7E11P, UNC93B1, 23 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
    nsv6309379copy number variation1nstd102humanUncertain significance GRCh37 chr11: 67,759,017-67,761,285 , GRCh38.p12 chr11: 67,991,546-67,993,814 UNC93B1
    nsv6248164mobile element insertion1nstd215human GRCh38 chr11: 67,997,232-67,997,232 , GRCh37.p13 chr11: 67,764,703-67,764,703 UNC93B1
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