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Items: 1 to 20 of 144

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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
    nsv5564399copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,192,101-8,283,260 , GRCh38.p12 chr17: 8,288,783-8,379,942 RANGRF, KRBA2, 5 more genes
    nsv5525019copy number variation1nstd206human GRCh38 chr17: 8,305,883-8,356,856 , GRCh37.p13 chr17: 8,209,201-8,260,174 ARHGEF15, ODF4, 1 more genes
    nsv5381042copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,212,556-8,226,834 , GRCh38.p12 chr17: 8,309,238-8,323,516 ARHGEF15
    nsv5157832mobile element insertion1nstd203human GRCh38 chr17: 8,308,643-8,308,659 , GRCh37.p13 chr17: 8,211,961-8,211,977 ARHGEF15
    nsv5023642copy number variation1nstd200human GRCh38 chr17: 8,317,815-8,352,755 , GRCh37.p13 chr17: 8,221,133-8,256,073 ARHGEF15, ODF4
    nsv5015782copy number variation1nstd200human GRCh38 chr17: 8,320,672-8,345,659 , GRCh37.p13 chr17: 8,223,990-8,248,977 ODF4, ARHGEF15
    nsv4864506copy number variation1nstd200human GRCh37 chr17: 8,209,201-8,260,174 , GRCh38.p12 chr17: 8,305,883-8,356,856 ARHGEF15, ODF4, 1 more genes
    nsv4857976copy number variation1nstd200human GRCh37 chr17: 8,223,237-8,223,352 , GRCh38.p12 chr17: 8,319,919-8,320,034 ARHGEF15
    nsv4857975copy number variation1nstd200human GRCh37 chr17: 8,212,653-8,213,123 , GRCh38.p12 chr17: 8,309,335-8,309,805 ARHGEF15
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4683837copy number variation2nstd102humanUncertain significance GRCh37 chr17: 8,131,488-8,285,638 , GRCh38.p12 chr17: 8,228,170-8,382,320 KRBA2, ARHGEF15, 7 more genes
    nsv4675487copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,937,691-8,247,776 , GRCh38.p12 chr17: 8,034,373-8,344,458 RANGRF, TRS-CGA1-1, 39 more genes
    nsv4621052copy number variation1nstd183human GRCh37 chr17: 8,210,352-8,253,984 , GRCh38.p12 chr17: 8,307,034-8,350,666 ODF4, ARHGEF15
    nsv4457674copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,676,383-8,350,870 , GRCh38.p12 chr17: 7,773,065-8,447,552 ARHGEF15, TRI-AAT4-1, 57 more genes
    nsv4454475copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,215,338-8,224,331 , GRCh38 chr17: 8,312,020-8,321,013 ARHGEF15
    nsv4453653copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,572,917-8,285,638 , GRCh38 chr17: 7,669,599-8,382,320 TRS-AGA2-6, ODF4, 59 more genes
    nsv4376992copy number variation1nstd173human GRCh37 chr17: 8,218,749-8,259,970 , GRCh38.p12 chr17: 8,315,431-8,356,652 LOC100128288, ARHGEF15, 1 more genes
    nsv4251687copy number variation1nstd166human GRCh37.p13 chr17: 8,223,237-8,223,352 , GRCh38.p12 chr17: 8,319,919-8,320,034 ARHGEF15
    nsv4248444copy number variation1nstd166human GRCh37.p13 chr17: 8,223,990-8,248,977 , GRCh38.p12 chr17: 8,320,672-8,345,659 ARHGEF15, ODF4
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