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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935905copy number variation1nstd209human GRCh38 chr17: 81,904,956-81,905,005 , GRCh37.p13 chr17: 79,862,832-79,862,881 PCYT2
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5295672copy number variation1nstd204human GRCh38.p13 chr17: 81,907,536-81,910,335 , GRCh37.p13 chr17: 79,865,412-79,868,211 PCYT2, SIRT7
    nsv5290477copy number variation1nstd204human GRCh38.p13 chr17: 81,742,501-82,145,800 , GRCh37.p13 chr17: 79,759,050-80,103,676 PPP1R27, MAFG, 27 more genes
    nsv5288922copy number variation1nstd204human GRCh37.p13 chr17: 79,777,077-79,870,376 , GRCh38.p13 chr17: 81,819,201-81,912,500 ARHGDIA, P4HB, 7 more genes
    nsv5017079copy number variation1nstd200human GRCh38 chr17: 81,903,984-81,904,584 , GRCh37.p13 chr17: 79,861,860-79,862,460 PCYT2
    nsv5017078copy number variation1nstd200human GRCh38 chr17: 81,903,669-81,922,080 , GRCh37.p13 chr17: 79,861,545-79,879,956 SIRT7, PCYT2, 1 more genes
    nsv4867546copy number variation1nstd200human GRCh37 chr17: 79,861,545-79,879,956 , GRCh38.p12 chr17: 81,903,669-81,922,080 SIRT7, MAFG, 1 more genes
    nsv4619638copy number variation1nstd183human GRCh37 chr17: 79,785,999-81,060,000 , GRCh38.p12 chr17: 81,828,123-83,101,964 , PCYT2, 55 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457495copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,663,313-80,197,463 , GRCh38.p12 chr17: 81,696,283-82,239,587 NOTUM, PPP1R27, 34 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3914754copy number variation1nstd102humanBenign GRCh37 chr17: 79,817,564-79,975,488 , GRCh38 chr17: 81,859,688-82,017,612 , NCBI36 chr17: 77,410,853-77,568,777 LOC105371939, NOTUM, 13 more genes
    nsv3914738copy number variation1nstd102humanPathogenic NCBI36 chr17: 74,409,636-78,637,842 , GRCh37 chr17: 76,898,041-81,044,553 , GRCh38 chr17: 78,901,959-83,086,677 MIR338, DUS1L, 127 more genes
    nsv3913720copy number variation1nstd102humanPathogenic GRCh38 chr17: 81,008,196-83,102,584 , GRCh37 chr17: 78,981,996-81,048,189 , NCBI36 chr17: 76,596,591-78,653,749 LOC105376789, MIR4525, 89 more genes
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