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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5473084copy number variation1nstd206human GRCh38 chr6: 27,132,731-27,133,715 , GRCh37.p13 chr6: 27,100,510-27,101,494 H2BC11, H2AC11
    nsv5233032copy number variation1nstd204human GRCh38.p13 chr6: 27,132,956-27,135,464 , GRCh37.p13 chr6: 27,100,735-27,103,243 H2BC11, H2AC11
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4940503copy number variation1nstd200human GRCh38 chr6: 27,133,231-27,133,383 , GRCh37.p13 chr6: 27,101,010-27,101,162 H2AC11, H2BC11
    nsv4940502copy number variation1nstd200human GRCh38 chr6: 27,132,141-27,134,626 , GRCh37.p13 chr6: 27,099,920-27,102,405 H2BC11, H2AC11
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    nsv4815706copy number variation1nstd200human GRCh37 chr6: 27,099,920-27,102,405 , GRCh38.p12 chr6: 27,132,141-27,134,626 H2AC11, H2BC11
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4592193copy number variation1nstd183human GRCh37 chr6: 27,099,872-27,115,362 , GRCh38.p12 chr6: 27,132,093-27,147,583 H4C9, H2AC11, 4 more genes
    nsv4381128copy number variation1nstd173human GRCh37 chr6: 26,941,502-27,391,254 , GRCh38.p12 chr6: 26,973,723-27,423,475 , RPL10P2, 45 more genes
    nsv3920564copy number variation1nstd102humanPathogenic GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946 PRELID1P2, RPL7AP7, 785 more genes
    nsv3913920copy number variation1nstd102humanPathogenic GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028 TRR-ACG1-2, TMEM217, 1385 more genes
    nsv3911053copy number variation1nstd102humanUncertain significance GRCh38 chr6: 26,280,579-28,727,313 , GRCh37 chr6: 26,280,807-28,695,090 , NCBI36 chr6: 26,388,786-28,803,069 GPX5, TRI-AAT9-1, 232 more genes
    nsv3889814copy number variation1nstd102humanPathogenic GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382 ITPR3, HSD17B8, 2905 more genes
    nsv3887898copy number variation2nstd102humanPathogenic GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394 SOD1P1, HLA-DPB1, 2905 more genes
    nsv3879811copy number variation1nstd102humanPathogenic GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083 RNU6-411P, LOC107986611, 2910 more genes
    nsv3877040copy number variation1nstd102humanPathogenic GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698 LOC105378061, MIR4640, 2914 more genes
    nsv3875385copy number variation1nstd102humanBenign GRCh37 chr6: 27,093,821-27,158,033 , GRCh38.p12 chr6: 27,126,042-27,190,254 H2AC12, TRH-GTG1-5, 8 more genes
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