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Items: 1 to 20 of 201

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5673052copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117 RPL23AP73, MIR195, 25 more genes
    nsv5593354copy number variation1nstd207human GRCh38 chr17: 7,205,695-7,205,751 , GRCh37.p13 chr17: 7,109,014-7,109,070 DLG4
    nsv5524989copy number variation1nstd206human GRCh38 chr17: 7,199,236-7,200,884 , GRCh37.p13 chr17: 7,102,555-7,104,203 DLG4
    nsv5518154copy number variation1nstd206human GRCh38 chr17: 7,200,922-7,654,532 , GRCh37.p13 chr17: 7,104,241-7,557,850 SNORA48, MPDU1-AS1, 47 more genes
    nsv5381181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,128,416 , GRCh38.p12 chr17: 6,425,460-7,225,097 RNA5SP435, RPL23AP73, 37 more genes
    nsv5290958copy number variation1nstd204human GRCh38.p13 chr17: 7,211,201-7,361,200 , GRCh37.p13 chr17: 7,114,520-7,264,519 ACADVL, ELP5, 15 more genes
    nsv5290585copy number variation1nstd204human GRCh38.p13 chr17: 7,132,501-7,211,000 , GRCh37.p13 chr17: 7,035,820-7,114,319 ASGR1, LOC105371512, 2 more genes
    nsv5283638copy number variation1nstd204human GRCh38.p13 chr17: 6,923,801-7,855,300 , GRCh37.p13 chr17: 6,827,120-7,758,618 , TNFSF12, 74 more genes
    nsv5015722copy number variation1nstd200human GRCh38 chr17: 7,199,244-7,201,153 , GRCh37.p13 chr17: 7,102,563-7,104,472 DLG4
    nsv5015721copy number variation1nstd200human GRCh38 chr17: 7,188,018-7,189,052 , GRCh37.p13 chr17: 7,091,337-7,092,371 DLG4
    nsv5015720copy number variation1nstd200human GRCh38 chr17: 7,187,490-7,189,040 , GRCh37.p13 chr17: 7,090,809-7,092,359 DLG4
    nsv5015719copy number variation1nstd200human GRCh38 chr17: 7,180,748-7,189,277 , GRCh37.p13 chr17: 7,084,067-7,092,596 DLG4
    nsv4857925copy number variation1nstd200human GRCh37 chr17: 7,090,809-7,092,359 , GRCh38.p12 chr17: 7,187,490-7,189,040 DLG4
    nsv4786168mobile element deletion1nstd200human GRCh37 chr17: 7,094,285-7,094,474 , GRCh38.p12 chr17: 7,190,966-7,191,155 DLG4
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4732188copy number variation1nstd199human GRCh37 chr17: 7,109,021-7,109,079 , GRCh38.p12 chr17: 7,205,702-7,205,760 DLG4
    nsv4729957copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,014,481-7,283,233 , GRCh38.p12 chr17: 7,111,162-7,379,914 MIR324, SLC2A4, 20 more genes
    nsv4729929copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,650,649-8,040,151 , GRCh38.p12 chr17: 6,747,330-8,136,833 CYB5D1, GPS2, 98 more genes
    nsv4683612copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,589,506-8,151,374 , GRCh38.p12 chr17: 6,686,187-8,248,056 ALOX12P2, DLG4, 124 more genes
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