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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5473492copy number variation1nstd206human GRCh38 chr6: 27,823,742-27,828,786 , GRCh37.p13 chr6: 27,791,520-27,796,564 H4C11
    nsv5466550copy number variation1nstd206human GRCh38 chr6: 27,711,907-27,849,290 , GRCh37.p13 chr6: 27,679,686-27,817,068 H4C11, H2AC13, 18 more genes
    nsv5462086copy number variation1nstd206human GRCh38 chr6: 27,798,000-27,892,000 , GRCh37.p13 chr6: 27,765,779-27,859,778 H3C11, H3C10, 17 more genes
    nsv5223198copy number variation1nstd204human GRCh38.p13 chr6: 27,740,101-28,055,500 , GRCh37.p13 chr6: 27,707,880-28,023,278 H2AC13, H2AC16, 35 more genes
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 more genes
    nsv4934552copy number variation1nstd200human GRCh38 chr6: 27,753,532-28,002,887 , GRCh37.p13 chr6: 27,721,311-27,970,665 TRX-CAT1-7, H3C10, 31 more genes
    nsv4879678inversion1nstd200human GRCh37 chr6: 25,888,654-29,672,093 , GRCh38.p12 chr6: 25,888,426-29,704,316 , H1-4, 368 more genes
    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
    nsv4675044copy number variation1nstd102humanLikely benign GRCh37 chr6: 27,616,157-28,011,557 , GRCh38.p12 chr6: 27,648,378-28,043,779 H2BC16P, H2BC17, 46 more genes
    nsv4593460copy number variation1nstd183human GRCh37 chr6: 27,775,213-27,873,766 , GRCh38.p12 chr6: 27,807,435-27,905,988 H2BC17, H2BC16P, 20 more genes
    nsv4592241copy number variation1nstd183human GRCh37 chr6: 27,792,261-27,802,580 , GRCh38.p12 chr6: 27,824,483-27,834,802 H4C11, H4C12
    nsv4490170mobile element insertion1nstd166human GRCh37.p13 chr6: 27,791,104-27,791,104 , GRCh38.p12 chr6: 27,823,326-27,823,326 H4C11
    nsv4434899copy number variation1nstd172human GRCh38.p12 chr6: 27,807,223-27,839,222 , GRCh37.p13 chr6: 27,775,001-27,807,000 H2AC13, H2AC15, 8 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
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