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Items: 1 to 20 of 167

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5672415inversion1nstd207human GRCh38 chr10: 79,542,902-80,213,948 , GRCh37.p13 chr10: 81,302,658-81,973,704 , ANXA11, 30 more genes
    nsv5627898insertion1nstd207human GRCh38 chr10: 79,918,997-79,918,997 , GRCh37.p13 chr10: 81,678,753-81,678,753 BMS1P21, MBL1P
    nsv5563886sequence alteration1nstd206human GRCh38 chr10: 79,543,104-80,217,086 , GRCh37.p13 chr10: 81,302,860-81,976,842 , ANXA11, 30 more genes
    nsv5483974copy number variation1nstd206human GRCh38 chr10: 79,796,368-80,226,368 , GRCh37.p13 chr10: 81,556,124-81,986,124 LOC642361, C1DP2, 20 more genes
    nsv5479685copy number variation1nstd206human GRCh38 chr10: 79,846,368-80,228,368 , GRCh37.p13 chr10: 81,606,124-81,988,124 ZNRF2P3, LINC00857, 18 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4729484copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673 DPY19L2P5, TSPAN14-AS1, 115 more genes
    nsv4729317copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023 LOC105378390, LRIT1, 109 more genes
    nsv4729258copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,457,752-81,990,746 , GRCh38.p12 chr10: 79,697,996-80,230,990 RPL22P18, MBL1P, 21 more genes
    nsv4729182copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,028,088-82,059,110 , GRCh38.p12 chr10: 79,268,331-80,299,354 SFTPA1, RPS12P18, 40 more genes
    nsv4728260copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943 C1DP3, RNA5SP322, 109 more genes
    nsv4606368copy number variation1nstd183human GRCh37 chr10: 81,672,312-81,679,489 , GRCh38.p12 chr10: 79,912,556-79,919,733 BMS1P21, MBL1P
    nsv4605455copy number variation1nstd183human GRCh37 chr10: 81,562,187-81,985,364 , GRCh38.p12 chr10: 79,802,431-80,225,608 LINC00857, ZNRF2P3, 20 more genes
    nsv4436457copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,630,953-81,966,548 , GRCh38.p12 chr10: 79,871,197-80,206,792 C1DP4, PGGT1BP2, 14 more genes
    nsv4430464copy number variation1nstd174human GRCh37 chr10: 81,672,066-81,679,878 , GRCh38.p12 chr10: 79,912,310-79,920,122 BMS1P21, MBL1P
    nsv4428976copy number variation1nstd174human GRCh37 chr10: 81,644,080-81,858,791 , GRCh38.p12 chr10: 79,884,324-80,099,035 SFTPD, TMEM254, 9 more genes
    nsv4425621copy number variation1nstd174human GRCh37 chr10: 81,682,942-81,972,386 , GRCh38.p12 chr10: 79,923,186-80,212,630 PLAC9, C1DP3, 12 more genes
    nsv4423759copy number variation1nstd174human GRCh37 chr10: 81,561,459-81,679,541 , GRCh38.p12 chr10: 79,801,703-79,919,785 MBL1P, NUTM2E, 7 more genes
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