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Items: 1 to 20 of 287

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978296inversion1nstd209human GRCh38 chr17: 81,945,255-82,544,213 , GRCh37.p13 chr17: 79,903,131-80,502,089 , CD7, 29 more genes
    nsv5943347copy number variation1nstd209human GRCh38 chr17: 82,053,771-82,054,039 , GRCh37.p13 chr17: 80,011,647-80,011,915 GPS1
    nsv5879375copy number variation1nstd209human GRCh38 chr17: 82,042,540-82,069,098 , GRCh37.p13 chr17: 80,000,416-80,026,974 RFNG, DUS1L, 1 more genes
    nsv5556495sequence alteration1nstd206human GRCh38 chr17: 81,945,298-82,544,214 , GRCh37.p13 chr17: 79,903,174-80,502,090 , RAC3, 29 more genes
    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
    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
    nsv4633985copy number variation1nstd183human GRCh37 chr17: 80,009,131-80,009,477 , GRCh38.p12 chr17: 82,051,255-82,051,601 RFNG, GPS1
    nsv4629184copy number variation1nstd183human GRCh37 chr17: 79,981,915-80,146,485 , GRCh38.p12 chr17: 82,024,039-82,188,609 RAC3, DCXR-DT, 8 more genes
    nsv4626485copy number variation2nstd183human GRCh37 chr17: 80,009,131-80,009,242 , GRCh38.p12 chr17: 82,051,255-82,051,366 GPS1, RFNG
    nsv4621153copy number variation1nstd183human GRCh37 chr17: 80,009,131-80,010,356 , GRCh38.p12 chr17: 82,051,255-82,052,480 GPS1, RFNG
    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
    nsv4269043copy number variation1nstd166human GRCh37.p13 chr17: 79,906,988-80,794,330 , GRCh38.p12 chr17: 81,949,112-82,836,454 , NOTUM, 39 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
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