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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380762copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-45,898,712 , GRCh38.p12 chr15: 44,563,121-45,606,514 LOC100533853, RNU6-1108P, 44 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5337311translocation1nstd200human GRCh37 chr15: 45,006,045-45,006,045 , GRCh37 chr15: 45,186,663-45,186,663 , GRCh38.p12 chr15|NT_187605.1: 37,193-37,193 , GRCh38.p12 chr15: 44,894,465-44,894,465 , GRCh38.p12 chr15|NT_187605.1: 226,329-226,329 , GRCh38.p12 chr15: 44,713,847-44,713,847 B2M
    nsv5328843translocation1nstd204human GRCh38.p13 chr15: 44,894,465-44,894,465 , GRCh38.p13 chr15: 44,713,847-44,713,847 , GRCh37.p13 chr15: 45,006,045-45,006,045 , GRCh37.p13 chr15: 45,186,663-45,186,663 B2M
    nsv5275882copy number variation1nstd204human GRCh38.p13 chr15: 44,713,839-44,731,682 , GRCh37.p13 chr15: 45,006,037-45,023,880 B2M, MIR10393, 1 more genes
    nsv5270030copy number variation1nstd204human GRCh38.p13 chr15: 44,714,801-44,824,200 , GRCh37.p13 chr15: 45,006,999-45,116,398 LOC100419583, MIR10393, 3 more genes
    nsv5269965copy number variation1nstd204human GRCh38.p13 chr15: 44,704,901-44,730,500 , GRCh37.p13 chr15: 44,997,099-45,022,698 B2M, PATL2, 2 more genes
    nsv5265834copy number variation1nstd204human GRCh38.p13 chr15: 44,713,989-44,812,174 , GRCh37.p13 chr15: 45,006,187-45,104,372 TRIM69, MIR10393, 2 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4682656copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,309-45,152,372 , GRCh38.p12 chr15|NT_187605.1: 1-192,038 , GRCh38.p12 chr15: 44,563,111-44,860,174 EIF3J, TRIM69, 7 more genes
    nsv4633766copy number variation1nstd183human GRCh37 chr15: 45,001,787-45,027,161 , GRCh38.p12 chr15: 44,709,589-44,734,963 , GRCh38.p12 chr15|NT_187605.1: 32,938-58,343 , B2M, 4 more genes
    nsv4632959copy number variation1nstd183human GRCh37 chr15: 44,956,586-45,027,161 , GRCh38.p12 chr15: 44,664,388-44,734,963 , GRCh38.p12 chr15|NT_187605.1: 1-58,343 , B2M, 4 more genes
    nsv4628238copy number variation1nstd183human GRCh37 chr15: 45,003,541-45,030,941 , GRCh38.p12 chr15: 44,711,343-44,738,743 , GRCh38.p12 chr15|NT_187605.1: 34,692-62,121 , B2M, 4 more genes
    nsv4621476copy number variation1nstd183human GRCh37 chr15: 44,972,024-45,040,431 , GRCh38.p12 chr15: 44,679,826-44,748,233 , GRCh38.p12 chr15|NT_187605.1: 3,163-71,611 , B2M, 4 more genes
    nsv4432230copy number variation1nstd172human GRCh38.p12 chr15: 44,710,803-44,736,802 , GRCh37.p13 chr15: 45,003,001-45,029,000 , GRCh38.p12 chr15|NT_187605.1: 34,152-60,179 , B2M, 4 more genes
    nsv4249483copy number variation1nstd166human GRCh37.p13 chr15: 45,001,000-45,007,000 , GRCh38.p12 chr15: 44,708,802-44,714,802 , GRCh38.p12 chr15|NT_187605.1: 32,151-38,148 , B2M, 1 more genes
    nsv4241918copy number variation1nstd166human GRCh37.p13 chr15: 44,998,000-45,024,000 , GRCh38.p12 chr15: 44,705,802-44,731,802 , GRCh38.p12 chr15|NT_187605.1: 29,139-55,183 , B2M, 3 more genes
    nsv3969464copy number variation1nstd168human GRCh38 chr15: 44,696,169-44,726,508 , GRCh37.p13 chr15: 44,988,367-45,018,706 B2M, PATL2, 1 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
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