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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906281copy number variation1nstd209human GRCh38 chr2: 151,374,868-151,379,127 , GRCh37.p13 chr2: 152,231,382-152,235,641 LOC101929319, TNFAIP6
    nsv5831865copy number variation1nstd209human GRCh38 chr2: 151,377,093-151,379,134 , GRCh37.p13 chr2: 152,233,607-152,235,648 LOC101929319, TNFAIP6
    nsv5690487mobile element insertion2nstd211human GRCh38 chr2: 151,377,636-151,377,636 , GRCh37.p13 chr2: 152,234,150-152,234,150 TNFAIP6, LOC101929319
    nsv5621119insertion1nstd207human GRCh38 chr2: 151,377,628-151,377,628 , GRCh37.p13 chr2: 152,234,142-152,234,142 LOC101929319, TNFAIP6
    nsv5571372copy number variation1nstd207human GRCh38 chr2: 151,370,439-151,370,534 , GRCh37.p13 chr2: 152,226,953-152,227,048 TNFAIP6, LOC101929319, 1 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5548596insertion1nstd206human GRCh38 chr2: 151,372,624-151,372,662 , GRCh37.p13 chr2: 152,229,138-152,229,176 TNFAIP6, LOC101929319, 1 more genes
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5444636copy number variation1nstd206human GRCh38 chr2: 150,863,589-152,862,185 , GRCh37.p13 chr2: 151,720,103-153,718,699 , CACNB4, 24 more genes
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5408974mobile element insertion1nstd206human GRCh38 chr2: 151,377,636-151,377,687 , GRCh37.p13 chr2: 152,234,150-152,234,201 TNFAIP6, LOC101929319
    nsv5381338copy number variation1nstd102humanPathogenic GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882 YY1P2, SPOPL, 156 more genes
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5079285mobile element insertion1nstd203human GRCh38 chr2: 151,377,633-151,377,636 , GRCh37.p13 chr2: 152,234,147-152,234,150 TNFAIP6, LOC101929319
    nsv5072388mobile element insertion1nstd203human GRCh38 chr2: 151,377,627-151,377,636 , GRCh37.p13 chr2: 152,234,141-152,234,150 LOC101929319, TNFAIP6
    nsv5068697mobile element insertion1nstd203human GRCh38 chr2: 151,377,632-151,377,636 , GRCh37.p13 chr2: 152,234,146-152,234,150 LOC101929319, TNFAIP6
    nsv5064140mobile element insertion1nstd203human GRCh38 chr2: 151,377,628-151,377,636 , GRCh37.p13 chr2: 152,234,142-152,234,150 LOC101929319, TNFAIP6
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4924119copy number variation1nstd200human GRCh38 chr2: 151,160,100-151,450,583 , GRCh37.p13 chr2: 152,016,614-152,307,097 FABP5P10, RBM43, 9 more genes
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