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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072883inversion1nstd229human GRCh38 chr10: 9,522,603-10,253,731 , GRCh37.p13 chr10: 9,564,566-10,295,694 LINC02663, HSP90AB7P, 3 more genes
    nsv7061558inversion1nstd229human GRCh38 chr10: 10,028,466-10,175,486 , GRCh37.p13 chr10: 10,070,429-10,217,449 LINC02670, ELOCP3
    nsv6891047copy number variation1nstd229human GRCh38 chr10: 9,379,303-10,380,878 , GRCh37.p13 chr10: 9,421,266-10,422,841 LOC107984207, LINC02670, 5 more genes
    nsv6889733copy number variation1nstd229human GRCh38 chr10: 10,029,801-10,085,200 , GRCh37.p13 chr10: 10,071,764-10,127,163 LINC02670
    nsv6637939copy number variation1nstd102humanUncertain significance GRCh37 chr10: 100,027-12,648,149 , GRCh38.p12 chr10: 54,087-12,606,150 LARP4B-DT, CALML5, 206 more genes
    nsv6637674copy number variation1nstd102humanUncertain significance GRCh37 chr10: 7,636,590-11,590,970 , GRCh38.p12 chr10: 7,594,627-11,548,971 HSP90AB7P, LOC105376394, 41 more genes
    nsv6450166copy number variation1nstd223human GRCh38 chr10: 10,059,256-10,059,782 , GRCh37.p13 chr10: 10,101,219-10,101,745 LINC02670
    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
    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
    nsv4679560copy number variation1nstd189human GRCh37.p13 chr10: 9,302,856-10,277,312 , GRCh38.p12 chr10: 9,260,893-10,235,349 , HSP90AB7P, 6 more genes
    nsv4614803copy number variation1nstd183human GRCh37 chr10: 9,852,654-10,718,325 , GRCh38.p12 chr10: 9,810,691-10,676,362 CELF2, ELOCP3, 6 more genes
    nsv4456951copy number variation1nstd102humanUncertain significance GRCh37 chr10: 9,996,504-10,689,065 , GRCh38.p12 chr10: 9,954,541-10,647,102 CELF2, CELF2-DT, 4 more genes
    nsv4455607copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,026-15,273,144 , GRCh38.p12 chr10: 54,086-15,231,145 LOC105376357, LINC02649, 264 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv3966283copy number variation1nstd168human GRCh38 chr10: 10,046,256-10,073,867 , GRCh37.p13 chr10: 10,088,219-10,115,830 LINC02670
    nsv3924406copy number variation1nstd102humanPathogenic GRCh38 chr10: 69,261-19,184,047 , GRCh37 chr10: 224,406-19,472,976 , NCBI36 chr10: 105,201-19,512,982 WDR37, LOC105376364, 302 more genes
    nsv3923974copy number variation1nstd102humanPathogenic NCBI36 chr10: 109,796-12,897,920 , GRCh38 chr10: 73,856-12,815,915 , GRCh37 chr10: 119,796-12,857,914 LINC02663, LARP4B-DT, 208 more genes
    nsv3922639copy number variation1nstd102humanUncertain significance NCBI36 chr10: 10,053,063-10,692,804 , GRCh37 chr10: 10,013,057-10,652,798 , GRCh38 chr10: 9,971,094-10,610,835 CELF2-DT, LOC107984207, 4 more genes
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