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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5914456copy number variation1nstd209human GRCh38 chr7: 128,499,704-128,999,795 , GRCh37.p13 chr7: 128,139,758-128,639,849 , KCP, 25 more genes
    nsv5911338copy number variation1nstd209human GRCh38 chr7: 128,499,612-128,999,703 , GRCh37.p13 chr7: 128,139,666-128,639,757 , CICP14, 25 more genes
    nsv5910382copy number variation1nstd209human GRCh38 chr7: 128,864,765-128,864,820 , GRCh37.p13 chr7: 128,504,819-128,504,874 SPMIP1, ATP6V1F
    nsv5627772insertion1nstd207human GRCh38 chr7: 128,864,765-128,864,765 , GRCh37.p13 chr7: 128,504,819-128,504,819 ATP6V1F, SPMIP1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4968742copy number variation1nstd200human GRCh38 chr7: 128,860,771-128,872,563 , GRCh37.p13 chr7: 128,500,825-128,512,617 ATP6V1F, FLNC-AS1, 2 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4602823copy number variation1nstd183human GRCh37 chr7: 128,418,055-128,592,817 , GRCh38.p12 chr7: 128,778,001-128,952,763 , LOC105375497, 10 more genes
    nsv4543506insertion1nstd166human GRCh37.p13 chr7: 128,504,819-128,504,819 , GRCh38.p12 chr7: 128,864,765-128,864,765 SPMIP1, ATP6V1F
    nsv4540359insertion1nstd166human GRCh37.p13 chr7: 128,504,797-128,504,797 , GRCh38.p12 chr7: 128,864,743-128,864,743 ATP6V1F, SPMIP1
    nsv4524679copy number variation1nstd166human GRCh37.p13 chr7: 128,504,819-128,504,912 , GRCh38.p12 chr7: 128,864,765-128,864,858 ATP6V1F, SPMIP1
    nsv4456996copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,412,321-128,546,131 , GRCh38.p12 chr7: 128,772,267-128,906,078 CALU, TRP-AGG2-3, 8 more genes
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4398959copy number variation1nstd174human GRCh37 chr7: 128,139,494-128,639,727 , GRCh38.p12 chr7: 128,499,440-128,999,673 , RNA5SP242, 25 more genes
    nsv4394893copy number variation1nstd174human GRCh37 chr7: 128,468,001-128,502,400 , GRCh38.p12 chr7: 128,827,947-128,862,346 FLNC-AS1, FLNC, 1 more genes
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