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Items: 1 to 20 of 268

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7071514inversion1nstd229human GRCh38 chr11: 67,656,060-67,862,553 , GRCh37.p13 chr11: 67,423,531-67,630,024 ENPP7P7, OR7E145P, 8 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
    nsv6916749copy number variation1nstd229human GRCh38 chr11: 67,715,101-67,740,000 , GRCh37.p13 chr11: 67,482,572-67,507,471 OR7E11P, UNC93B5, 1 more genes
    nsv6912914copy number variation1nstd229human GRCh38 chr11: 67,707,301-67,987,215 , GRCh37.p13 chr11: 67,474,772-67,754,686 SNRPCP12, UNC93B5, 13 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
    nsv6912177copy number variation1nstd229human GRCh38 chr11: 67,717,001-67,745,100 , GRCh37.p13 chr11: 67,484,472-67,512,571 OR7E11P, OR7E145P
    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
    nsv6908684copy number variation1nstd229human GRCh38 chr11: 67,708,412-67,988,340 , GRCh37.p13 chr11: 67,475,883-67,755,811 ALG1L8P, LOC112268076, 13 more genes
    nsv6907873copy number variation1nstd229human GRCh38 chr11: 67,717,301-67,742,400 , GRCh37.p13 chr11: 67,484,772-67,509,871 OR7E145P, OR7E11P
    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
    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
    nsv6903373copy number variation1nstd229human GRCh38 chr11: 67,717,601-67,742,200 , GRCh37.p13 chr11: 67,485,072-67,509,671 OR7E11P, OR7E145P
    nsv6902512copy number variation1nstd229human GRCh38 chr11: 67,714,901-67,740,100 , GRCh37.p13 chr11: 67,482,372-67,507,571 OR7E145P, UNC93B5, 1 more genes
    nsv6902419copy number variation1nstd229human GRCh38 chr11: 67,716,664-67,739,583 , GRCh37.p13 chr11: 67,484,135-67,507,054 OR7E11P, OR7E145P
    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
    nsv6901287copy number variation1nstd229human GRCh38 chr11: 67,715,901-67,740,200 , GRCh37.p13 chr11: 67,483,372-67,507,671 OR7E145P, UNC93B5, 1 more genes
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