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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5885205copy number variation1nstd209human GRCh38 chr17: 5,014,139-5,016,302 , GRCh37.p13 chr17: 4,917,434-4,919,597 KIF1C
    nsv5880181copy number variation1nstd209human GRCh38 chr17: 5,021,725-5,022,795 , GRCh37.p13 chr17: 4,925,020-4,926,090 KIF1C
    nsv5525997copy number variation1nstd206human GRCh38 chr17: 5,016,526-5,017,592 , GRCh37.p13 chr17: 4,919,821-4,920,887 KIF1C, KIF1C-AS1
    nsv5283967copy number variation1nstd204human GRCh38.p13 chr17: 4,830,501-5,066,500 , GRCh37.p13 chr17: 4,733,796-4,969,795 , RN7SL784P, 20 more genes
    nsv5142160mobile element insertion1nstd203human GRCh38 chr17: 5,028,785-5,028,807 , GRCh37.p13 chr17: 4,932,080-4,932,102 , KIF1C, 1 more genes
    nsv4857837copy number variation1nstd200human GRCh37 chr17: 4,917,160-4,917,766 , GRCh38.p12 chr17: 5,013,865-5,014,471 KIF1C
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4735691copy number variation1nstd199human GRCh37 chr17: 4,912,931-4,913,006 , GRCh38.p12 chr17: 5,009,636-5,009,711 KIF1C
    nsv4683556copy number variation2nstd102humanUncertain significance GRCh37 chr17: 4,802,021-4,927,456 , GRCh38.p12 chr17: 4,898,726-5,024,161 CHRNE, SPAG7, 13 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4634092copy number variation1nstd183human GRCh37 chr17: 4,923,889-4,924,153 , GRCh38.p12 chr17: 5,020,594-5,020,858 KIF1C
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4623794copy number variation1nstd183human GRCh37 chr17: 4,900,910-4,901,361 , GRCh38.p12 chr17: 4,997,615-4,998,066 INCA1, KIF1C
    nsv4574293mobile element insertion1nstd166human GRCh37.p13 chr17: 4,920,896-4,920,896 , GRCh38.p12 chr17: 5,017,601-5,017,601 KIF1C, KIF1C-AS1
    nsv4532087copy number variation1nstd166human GRCh37.p13 chr17: 4,896,999-4,955,000 , GRCh38.p12 chr17: 4,993,704-5,051,705 , KIF1C, 4 more genes
    nsv4457731copy number variation1nstd102humanUncertain significance GRCh37 chr17: 4,845,435-5,097,302 , GRCh38.p12 chr17: 4,942,140-5,194,007 ZNF594, ZNF232, 18 more genes
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv4247294copy number variation1nstd166human GRCh37.p13 chr17: 4,901,262-4,901,321 , GRCh38.p12 chr17: 4,997,967-4,998,026 KIF1C, INCA1
    nsv4244582copy number variation1nstd166human GRCh37.p13 chr17: 4,924,589-4,924,702 , GRCh38.p12 chr17: 5,021,294-5,021,407 KIF1C
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