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Items: 1 to 20 of 113

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7073282inversion1nstd229human GRCh38 chr10: 12,099,288-14,830,781 , GRCh37.p13 chr10: 12,141,287-14,872,780 MIR1265, RNA5SP301, 45 more genes
    nsv7060184inversion1nstd229human GRCh38 chr10: 13,148,010-16,128,795 , GRCh37.p13 chr10: 13,190,010-16,170,794 LOC101928453, MCM10, 52 more genes
    nsv6897733copy number variation1nstd229human GRCh38 chr10: 14,809,152-14,886,833 , GRCh37.p13 chr10: 14,851,151-14,928,832 SUV39H2, CDNF, 2 more genes
    nsv6894787copy number variation1nstd229human GRCh38 chr10: 14,826,783-14,830,920 , GRCh37.p13 chr10: 14,868,782-14,872,919 CDNF
    nsv6584976inversion1nstd223human GRCh38 chr10: 14,820,531-14,821,175 , GRCh37.p13 chr10: 14,862,530-14,863,174 CDNF
    nsv6581078inversion1nstd223human GRCh38 chr10: 14,816,981-14,817,610 , GRCh37.p13 chr10: 14,858,980-14,859,609 CDNF
    nsv6313952copy number variation1nstd102humanPathogenic GRCh37 chr10: 6,273,934-34,732,521 , GRCh38.p12 chr10: 6,231,971-34,443,593 RPL36AP55, HNRNPA1P32, 418 more genes
    nsv6290893copy number variation1nstd102humannot provided GRCh37 chr10: 135,655-47,688,677 , GRCh38.p12 chr10: 89,715-47,923,579 C1QL3, LOC105376441, 774 more genes
    nsv6131971copy number variation1nstd213human GRCh37 chr10: 7,450,000-17,830,001 , GRCh38.p12 chr10: 7,408,038-17,788,002 ATP5F1C, TRDMT1, 150 more genes
    nsv5925366copy number variation1nstd209human GRCh38 chr10: 14,826,121-14,826,171 , GRCh37.p13 chr10: 14,868,120-14,868,170 CDNF
    nsv5917974copy number variation1nstd209human GRCh38 chr10: 14,826,002-14,826,521 , GRCh37.p13 chr10: 14,868,001-14,868,520 CDNF
    nsv5535134insertion1nstd206human GRCh38 chr10: 14,826,049-14,826,068 , GRCh37.p13 chr10: 14,868,048-14,868,067 CDNF
    nsv5381768copy number variation1nstd102humanPathogenic GRCh37 chr10: 9,137,489-17,227,168 , GRCh38.p12 chr10: 9,095,526-17,185,169 PROSER2, C1QL3, 110 more genes
    nsv5219127mobile element deletion1nstd204human GRCh38.p13 chr10: 14,830,555-14,830,883 , GRCh37.p13 chr10: 14,872,554-14,872,882 CDNF
    nsv4983785copy number variation1nstd200human GRCh38 chr10: 14,813,015-14,833,181 , GRCh37.p13 chr10: 14,855,014-14,875,180 CDNF
    nsv4846335copy number variation1nstd200human GRCh37 chr10: 14,855,014-14,875,180 , GRCh38.p12 chr10: 14,813,015-14,833,181 CDNF
    nsv4785836mobile element deletion1nstd200human GRCh37 chr10: 14,872,563-14,872,874 , GRCh38.p12 chr10: 14,830,564-14,830,875 CDNF
    nsv4679303copy number variation1nstd189human GRCh37.p13 chr10: 14,723,081-14,883,651 , GRCh38.p12 chr10: 14,681,082-14,841,652 HSPA14, FAM107B, 3 more genes
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