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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5686500mobile element insertion2nstd211human GRCh38 chr6: 28,569,704-28,569,704 , GRCh37.p13 chr6: 28,537,481-28,537,481 SCAND3
    nsv5471232copy number variation1nstd206human GRCh38 chr6: 28,557,707-28,888,244 , GRCh37.p13 chr6: 28,525,484-28,856,021 TRA-TGC5-1, TRA-AGC1-1, 33 more genes
    nsv5469905copy number variation1nstd206human GRCh38 chr6: 28,576,858-28,582,626 , GRCh37.p13 chr6: 28,544,635-28,550,403 SCAND3
    nsv5410833mobile element insertion1nstd206human GRCh38 chr6: 28,569,704-28,569,707 , GRCh37.p13 chr6: 28,537,481-28,537,484 SCAND3
    nsv5115708mobile element insertion1nstd203human GRCh38 chr6: 28,569,692-28,569,704 , GRCh37.p13 chr6: 28,537,469-28,537,481 SCAND3
    nsv5106217mobile element insertion1nstd203human GRCh38 chr6: 28,584,742-28,584,756 , GRCh37.p13 chr6: 28,552,519-28,552,533 SCAND3
    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
    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
    nsv4412700copy number variation1nstd174human GRCh37 chr6: 28,577,001-28,581,900 , GRCh38.p12 chr6: 28,609,224-28,614,123 SCAND3
    nsv4374377copy number variation1nstd173human GRCh37 chr6: 28,551,196-28,641,689 , GRCh38.p12 chr6: 28,583,419-28,673,912 TRA-CGC2-1, LOC105374996, 9 more genes
    nsv4365128copy number variation1nstd173human GRCh37 chr6: 28,567,231-28,649,125 , GRCh38.p12 chr6: 28,599,454-28,681,348 TRA-AGC4-1, TRA-TGC2-1, 7 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
    nsv3915580copy number variation1nstd102humanUncertain significance NCBI36 chr6: 28,516,623-28,779,629 , GRCh37.p13 chr6: 28,408,644-28,671,650 , GRCh38.p12 chr6: 28,440,867-28,703,873 SCAND3, TRK-TTT13-1, 24 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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