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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096652copy number variation1nstd102humanPathogenic GRCh37 chr2: 37,334,416-39,347,563 , GRCh38.p12 chr2: 37,107,273-39,120,422 RPL31P16, GALM, 52 more genes
    nsv6672695copy number variation1nstd229human GRCh38 chr2: 37,125,223-37,205,811 , GRCh37.p13 chr2: 37,352,366-37,432,954 SULT6B1, CEBPZOS, 4 more genes
    nsv6672497copy number variation1nstd229human GRCh38 chr2: 37,192,501-37,201,400 , GRCh37.p13 chr2: 37,419,644-37,428,543 RPL31P16, SULT6B1, 2 more genes
    nsv6664759copy number variation1nstd229human GRCh38 chr2: 37,215,219-37,215,393 , GRCh37.p13 chr2: 37,442,362-37,442,536 CEBPZOS, CEBPZ
    nsv6662758copy number variation1nstd229human GRCh38 chr2: 37,129,801-37,222,300 , GRCh37.p13 chr2: 37,356,944-37,449,443 RPL31P16, SULT6B1, 4 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6549542inversion1nstd223human GRCh38 chr2: 32,866,974-37,651,961 , GRCh37.p13 chr2: 33,092,041-37,879,104 QPCT, TYW1P1, 55 more genes
    nsv6548859inversion1nstd223human GRCh38 chr2: 32,866,975-38,526,880 , GRCh37.p13 chr2: 33,092,042-38,754,022 ATP6V0E1P3, ARL14EPP1, 76 more genes
    nsv6548072inversion1nstd223human GRCh38 chr2: 32,866,995-42,468,982 , GRCh37.p13 chr2: 33,092,062-42,696,122 PKDCC, SRSF7, 127 more genes
    nsv6544899inversion1nstd223human GRCh38 chr2: 32,866,958-38,386,116 , GRCh37.p13 chr2: 33,092,025-38,613,258 ATP6V0E1P3, H2ACP2, 72 more genes
    nsv6544571inversion1nstd223human GRCh38 chr2: 32,867,025-38,327,253 , GRCh37.p13 chr2: 33,092,092-38,554,395 MIR548AD, LOC107985870, 72 more genes
    nsv6542757inversion1nstd223human GRCh38 chr2: 32,866,974-42,451,061 , GRCh37.p13 chr2: 33,092,041-42,678,201 RASGRP3, TTC39DP, 125 more genes
    nsv6540167inversion1nstd223human GRCh38 chr2: 32,866,952-40,818,398 , GRCh37.p13 chr2: 33,092,019-41,045,538 CEBPZOS, RNU6-1116P, 110 more genes
    nsv6539485inversion1nstd223human GRCh38 chr2: 32,866,964-42,766,565 , GRCh37.p13 chr2: 33,092,031-42,993,705 RN7SL602P, RNU6-851P, 132 more genes
    nsv6538702inversion1nstd223human GRCh38 chr2: 37,202,648-37,204,386 , GRCh37.p13 chr2: 37,429,791-37,431,529 CEBPZOS, CEBPZ
    nsv6349429copy number variation1nstd223human GRCh38 chr2: 37,136,210-37,198,359 , GRCh37.p13 chr2: 37,363,353-37,425,502 EIF2AK2, RPL31P16, 3 more genes
    nsv6339101copy number variation1nstd223human GRCh38 chr2: 37,203,862-37,205,678 , GRCh37.p13 chr2: 37,431,005-37,432,821 CEBPZ, CEBPZOS
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313619copy number variation1nstd102humanPathogenic GRCh37 chr2: 29,899,368-42,441,440 , GRCh38.p12 chr2: 29,676,502-42,214,300 LOC107985870, SLC25A5P2, 161 more genes
    nsv6262155copy number variation1nstd214human GRCh38 chr2: 37,202,655-37,202,704 , GRCh37.p13 chr2: 37,429,798-37,429,847 CEBPZ, CEBPZOS
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