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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958936insertion1nstd209human GRCh38 chr2: 218,215,618-218,215,618 , GRCh37.p13 chr2: 219,080,341-219,080,341 LOC101928487, ARPC2
    nsv5896021copy number variation1nstd209human GRCh38 chr2: 218,230,288-218,232,545 , GRCh37.p13 chr2: 219,095,011-219,097,268 ARPC2
    nsv5679471mobile element insertion1nstd211human GRCh38 chr2: 218,242,754-218,242,754 , GRCh37.p13 chr2: 219,107,477-219,107,477 ARPC2
    nsv5621324insertion1nstd207human GRCh38 chr2: 218,235,237-218,235,237 , GRCh37.p13 chr2: 219,099,960-219,099,960 ARPC2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5443035copy number variation1nstd206human GRCh38 chr2: 218,238,797-218,238,872 , GRCh37.p13 chr2: 219,103,520-219,103,595 ARPC2
    nsv5441156copy number variation1nstd206human GRCh38 chr2: 218,142,455-218,226,626 , GRCh37.p13 chr2: 219,007,178-219,091,349 CXCR1, LOC101928487, 2 more genes
    nsv5434731copy number variation1nstd206human GRCh38 chr2: 218,230,268-218,232,589 , GRCh37.p13 chr2: 219,094,991-219,097,312 ARPC2
    nsv5409676mobile element insertion1nstd206human GRCh38 chr2: 218,242,754-218,242,805 , GRCh37.p13 chr2: 219,107,477-219,107,528 ARPC2
    nsv5303662copy number variation1nstd204human GRCh38.p13 chr2: 218,142,430-218,226,652 , GRCh37.p13 chr2: 219,007,153-219,091,375 LOC101928487, CXCR1, 2 more genes
    nsv5217153copy number variation1nstd204human GRCh38.p13 chr2: 218,230,291-218,232,433 , GRCh37.p13 chr2: 219,095,014-219,097,156 ARPC2
    nsv5210973copy number variation1nstd204human GRCh38.p13 chr2: 218,197,714-218,225,404 , GRCh37.p13 chr2: 219,062,437-219,090,127 HMGB1P9, ARPC2, 1 more genes
    nsv5205806copy number variation1nstd204human GRCh38.p13 chr2: 218,240,201-218,420,200 , GRCh37.p13 chr2: 219,104,924-219,284,923 CATIP, CATIP-AS1, 16 more genes
    nsv5203399copy number variation1nstd204human GRCh38.p13 chr2: 218,142,401-218,226,600 , GRCh37.p13 chr2: 219,007,124-219,091,323 HMGB1P9, LOC101928487, 2 more genes
    nsv5063945mobile element insertion1nstd203human GRCh38 chr2: 218,247,140-218,247,155 , GRCh37.p13 chr2: 219,111,863-219,111,878 ARPC2
    nsv5029880inversion1nstd200human GRCh38 chr2: 213,444,845-219,177,092 , GRCh37.p13 chr2: 214,309,569-220,041,814 , LOC102724861, 122 more genes
    nsv4913938copy number variation1nstd200human GRCh38 chr2: 218,252,508-218,258,498 , GRCh37.p13 chr2: 219,117,231-219,123,221 ARPC2, GPBAR1
    nsv4913937copy number variation1nstd200human GRCh38 chr2: 218,142,455-218,226,626 , GRCh37.p13 chr2: 219,007,178-219,091,349 HMGB1P9, LOC101928487, 2 more genes
    nsv4804623copy number variation1nstd200human GRCh37 chr2: 219,007,178-219,091,349 , GRCh38.p12 chr2: 218,142,455-218,226,626 HMGB1P9, ARPC2, 2 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
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