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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5925718copy number variation1nstd209human GRCh38 chr10: 69,149,997-69,150,307 , GRCh37.p13 chr10: 70,909,753-70,910,063 VPS26A
    nsv5704336mobile element insertion2nstd211human GRCh38 chr10: 69,144,740-69,144,740 , GRCh37.p13 chr10: 70,904,496-70,904,496 VPS26A
    nsv5411284mobile element insertion1nstd206human GRCh38 chr10: 69,144,740-69,144,791 , GRCh37.p13 chr10: 70,904,496-70,904,547 VPS26A
    nsv5347828translocation1nstd200human GRCh38 chr10: 69,124,146-69,124,146 , GRCh38 chr10: 69,124,040-69,124,040 , GRCh37.p13 chr10: 70,883,796-70,883,796 , GRCh37.p13 chr10: 70,883,902-70,883,902 VPS26A
    nsv5325283translocation1nstd204human GRCh38.p13 chr10: 69,124,040-69,124,040 , GRCh38.p13 chr10: 69,124,146-69,124,146 , GRCh37.p13 chr10: 70,883,902-70,883,902 , GRCh37.p13 chr10: 70,883,796-70,883,796 VPS26A
    nsv5125918mobile element insertion1nstd203human GRCh38 chr10: 69,144,723-69,144,740 , GRCh37.p13 chr10: 70,904,479-70,904,496 VPS26A
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4833851copy number variation1nstd200human GRCh37 chr10: 70,883,796-70,883,902 , GRCh38.p12 chr10: 69,124,040-69,124,146 VPS26A
    nsv4601421copy number variation1nstd183human GRCh37 chr10: 70,564,120-74,122,461 , GRCh38.p12 chr10: 68,804,363-72,362,703 , SGPL1, 79 more genes
    nsv4497819mobile element insertion1nstd166human GRCh37.p13 chr10: 70,904,479-70,904,479 , GRCh38.p12 chr10: 69,144,723-69,144,723 VPS26A
    nsv4343722sequence alteration1nstd166human GRCh37.p13 chr10: 43,905,894-92,001,956 , GRCh38.p12 chr10: 43,410,446-90,242,199 , ALOX5, 749 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
    nsv4184699copy number variation1nstd166human GRCh37.p13 chr10: 70,878,000-70,889,000 , GRCh38.p12 chr10: 69,118,244-69,129,244 VPS26A
    nsv3959237insertion1nstd168human GRCh38 chr10: 69,094,031-69,125,150 , GRCh37.p13 chr10: 70,853,787-70,884,906 SRGN, VPS26A
    nsv3924859copy number variation1nstd102humanPathogenic NCBI36 chr10: 52,159,133-88,896,941 , GRCh38 chr10: 50,729,367-87,147,204 , GRCh37 chr10: 52,489,127-88,906,961 BMS1P4-AGAP5, MTCO2P23, 471 more genes
    nsv3922335copy number variation1nstd102humanPathogenic GRCh37 chr10: 60,196,226-76,174,974 , GRCh38 chr10: 58,436,466-74,415,216 , NCBI36 chr10: 59,866,232-75,844,980 UNC5B-AS1, ALDH7A1P4, 250 more genes
    nsv3917966copy number variation1nstd102humanPathogenic NCBI36 chr10: 68,626,331-80,851,819 , GRCh37 chr10: 68,956,325-81,181,813 , GRCh38 chr10: 67,196,567-79,422,057 LINC02640, HK1, 231 more genes
    nsv3917822copy number variation1nstd102humanPathogenic GRCh38 chr10: 63,402,579-75,296,099 , GRCh37 chr10: 65,162,339-77,055,857 , NCBI36 chr10: 64,832,345-76,725,863 MYL6P3, CHCHD1, 220 more genes
    nsv3917047copy number variation1nstd102humanPathogenic NCBI36 chr10: 42,500,760-75,145,672 , GRCh37 chr10: 43,180,754-75,475,666 , GRCh38 chr10: 42,685,306-73,715,908 SLC9A3P3, JMJD1C-AS2, 476 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
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