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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964362insertion1nstd209human GRCh38 chr2: 170,781,736-170,781,736 , GRCh37.p13 chr2: 171,638,246-171,638,246 ERICH2
    nsv5621280insertion1nstd207human GRCh38 chr2: 170,781,736-170,781,736 , GRCh37.p13 chr2: 171,638,246-171,638,246 ERICH2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 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
    nsv5546970insertion1nstd206human GRCh38 chr2: 170,781,749-170,781,787 , GRCh37.p13 chr2: 171,638,259-171,638,297 ERICH2
    nsv5451100copy number variation1nstd206human GRCh38 chr2: 170,769,093-170,769,167 , GRCh37.p13 chr2: 171,625,603-171,625,677 ERICH2-DT, ERICH2
    nsv5176364mobile element insertion1nstd203human GRCh38 chr2: 170,779,883-170,779,897 , GRCh37.p13 chr2: 171,636,393-171,636,407 ERICH2
    nsv5074049mobile element insertion1nstd203human GRCh38 chr2: 170,776,211-170,776,220 , GRCh37.p13 chr2: 171,632,721-171,632,730 ERICH2
    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
    nsv4926473copy number variation1nstd200human GRCh38 chr2: 170,780,808-170,783,947 , GRCh37.p13 chr2: 171,637,318-171,640,457 ERICH2
    nsv4926472copy number variation1nstd200human GRCh38 chr2: 170,757,709-170,781,473 , GRCh37.p13 chr2: 171,614,219-171,637,983 ERICH2-DT, ERICH2
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4789888copy number variation1nstd200human GRCh37 chr2: 171,637,318-171,640,457 , GRCh38.p12 chr2: 170,780,808-170,783,947 ERICH2
    nsv4768307copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,078,055-182,119,617 , GRCh38.p12 chr2: 162,221,545-181,254,890 RBM45, LOC102724194, 258 more genes
    nsv4760589insertion1nstd199human GRCh37 chr2: 171,638,255-171,638,255 , GRCh38.p12 chr2: 170,781,745-170,781,745 ERICH2
    nsv4725788insertion1nstd186human GRCh37 chr2: 171,638,246-171,638,246 , GRCh38.p12 chr2: 170,781,736-170,781,736 ERICH2
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4582745copy number variation1nstd183human GRCh37 chr2: 171,633,674-171,633,879 , GRCh38.p12 chr2: 170,777,164-170,777,369 ERICH2
    nsv4552823insertion1nstd166human GRCh37.p13 chr2: 171,638,246-171,638,246 , GRCh38.p12 chr2: 170,781,736-170,781,736 ERICH2
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