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Items: 1 to 20 of 7097

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6131281insertion1nstd186human GRCh37 chr22: 31,622,461-31,622,461 , GRCh38.p12 chr22: 31,226,475-31,226,475 LIMK2
    nsv6124744copy number variation1nstd186human GRCh37 chr18: 3,272,249-3,272,300 , GRCh38.p12 chr18: 3,272,251-3,272,302 MYL12B
    nsv6119969copy number variation1nstd186human GRCh37 chr1: 22,420,791-22,421,089 , GRCh38.p12 chr1: 22,094,298-22,094,596 CDC42
    nsv6117186mobile element insertion1nstd186human GRCh37 chr22: 36,711,883-36,711,928 , GRCh38.p12 chr22: 36,315,838-36,315,883 MYH9
    nsv6112816copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16|NT_187607.1: 326,909-1,872,893 NTAN1, MIR3179-1, 50 more genes
    nsv6112795copy number variation1nstd102humanPathogenic GRCh37 chr18: 64,996-6,838,315 , GRCh38.p12 chr18: 64,996-6,838,316 TYMSOS, LOC107985176, 104 more genes
    nsv6112786copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,124,782-16,291,779 , GRCh38.p12 chr16: 15,030,925-16,197,922 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-1,855,918 RNU6-213P, LOC105371102, 25 more genes
    nsv5980403copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr16: 15,802,668-15,932,109 , GRCh38.p12 chr16|NT_187607.1: 1,366,822-1,496,241 , GRCh38.p12 chr16: 15,708,811-15,838,252 NDE1, MYH11
    nsv5977796inversion1nstd209human GRCh38 chr1: 22,029,244-22,112,233 , GRCh37.p13 chr1: 22,355,737-22,438,726 CDC42, LINC00339, 2 more genes
    nsv5977771inversion1nstd209human GRCh38 chr18: 21,077,777-21,079,358 , GRCh37.p13 chr18: 18,657,738-18,659,319 ROCK1
    nsv5977357insertion1nstd209human GRCh38 chr22: 36,315,826-36,315,826 , GRCh37.p13 chr22: 36,711,871-36,711,871 MYH9
    nsv5977280insertion1nstd209human GRCh38 chr16: 15,821,935-15,821,935 , GRCh37.p13 chr16: 15,915,792-15,915,792 MYH11
    nsv5976512inversion1nstd209human GRCh38 chr7: 5,976,108-6,745,714 , GRCh37.p13 chr7: 6,015,739-6,785,345 PMS2, RAC1, 22 more genes
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5972667insertion1nstd209human GRCh38 chr22: 36,384,612-36,384,612 , GRCh37.p13 chr22: 36,780,657-36,780,657 MYH9
    nsv5971690insertion1nstd209human GRCh38 chr17: 8,499,874-8,499,874 , GRCh37.p13 chr17: 8,403,192-8,403,192 MYH10
    nsv5970939insertion1nstd209human GRCh38 chr17: 39,724,272-39,724,272 , GRCh37.p13 chr17: 37,880,525-37,880,525 ERBB2
    nsv5970917insertion1nstd209human GRCh38 chr17: 8,489,708-8,489,708 , GRCh37.p13 chr17: 8,393,026-8,393,026 MYH10
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