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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
    nsv5968268inversion1nstd209human GRCh38 chr6: 28,831,490-29,349,953 , GRCh37.p13 chr6: 28,799,267-29,317,730 KRT18P1, TRIM27, 44 more genes
    nsv5036471inversion1nstd200human GRCh38 chr6: 25,888,426-29,704,316 , GRCh37.p13 chr6: 25,888,654-29,672,093 , OR11A1, 368 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
    nsv4815761copy number variation1nstd200human GRCh37 chr6: 28,912,359-28,912,745 , GRCh38.p12 chr6: 28,944,582-28,944,968 LINC01556, TRM-CAT3-1
    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
    nsv4680813copy number variation1nstd189human GRCh37.p13 chr6: 28,900,618-29,292,087 , GRCh38.p12 chr6: 28,932,841-29,324,310 KRT18P1, OR2W1, 33 more genes
    nsv4679405copy number variation1nstd189human GRCh37.p13 chr6: 28,808,718-28,956,583 , GRCh38.p12 chr6: 28,840,941-28,988,806 KRT18P1, TRIM27, 20 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
    nsv3918042copy number variation1nstd102humanUncertain significance NCBI36 chr6: 28,987,399-29,465,533 , GRCh37.p13 chr6|NT_167245.1: 245,961-622,457 , GRCh37.p13 chr6|NT_167247.1: 186,758-635,908 , GRCh37.p13 chr6|NT_167249.1: 233,223-673,240 , GRCh37.p13 chr6|NT_167246.1: 184,244-635,721 , GRCh37.p13 chr6: 28,879,420-29,357,554 , GRCh38.p12 chr6: 28,911,643-29,389,777 , GRCh38.p12 chr6|NT_167247.2: 181,174-630,323 , GRCh38.p12 chr6|NT_167249.2: 233,925-673,942 , GRCh38.p12 chr6|NT_167245.2: 240,377-616,872 , GRCh38.p12 chr6|NT_167246.2: 178,625-630,101 ZNF311, OR14J1, 38 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
    nsv3912336copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,730,964-29,737,605 , GRCh38 chr6: 28,763,187-29,769,828 , NCBI36 chr6: 28,838,943-29,845,584 OR2AD1P, UBD, 87 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
    nsv3888352copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,735,761-29,585,573 , GRCh38.p12 chr6: 28,767,984-29,617,796 OR12D1, LOC105379641, 75 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
    nsv3870570copy number variation1nstd102humanUncertain significance GRCh37 chr6: 28,130,359-32,108,367 , GRCh38.p12 chr6: 28,162,581-32,140,590 LOC105375002, SKIC2, 345 more genes
    nsv3169066inversion1nstd158human GRCh37 chr6: 5,923,377-99,717,885 , GRCh38.p12 chr6: 5,923,144-99,270,009 , ABCF1, 1877 more genes
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