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Items: 1 to 20 of 285

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5831496copy number variation2nstd209human GRCh38 chr2: 131,457,022-131,459,836 , GRCh37.p13 chr2: 132,214,595-132,217,409 RHOQP2
    nsv5831294copy number variation2nstd209human GRCh38 chr2: 131,460,131-131,462,711 , GRCh37.p13 chr2: 132,217,704-132,220,284 RHOQP2
    nsv5665937inversion1nstd207human GRCh38 chr2: 130,138,213-131,531,319 , GRCh37.p13 chr2: 130,895,786-132,288,892 , GNAQP1, 84 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 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
    nsv5449829copy number variation1nstd206human GRCh38 chr2: 131,463,618-131,474,000 , GRCh37.p13 chr2: 132,221,191-132,231,573 RHOQP2, MZT2A
    nsv5449752copy number variation1nstd206human GRCh38 chr2: 131,233,309-131,501,809 , GRCh37.p13 chr2: 131,990,882-132,259,177 SMPD4BP, MTND3P18, 31 more genes
    nsv5439461copy number variation1nstd206human GRCh38 chr2: 131,381,309-131,531,618 , GRCh37.p13 chr2: 132,138,882-132,289,191 MTCO2P18, LOC112268425, 17 more genes
    nsv5437602copy number variation1nstd206human GRCh38 chr2: 131,208,309-131,740,809 , GRCh37.p13 chr2: 131,965,882-132,498,382 , LINC01120, 42 more genes
    nsv5434286copy number variation1nstd206human GRCh38 chr2: 131,208,118-131,540,100 , GRCh37.p13 chr2: 131,965,691-132,297,673 , MTND2P18, 35 more genes
    nsv5327037inversion1nstd204human GRCh37.p13 chr2: 130,942,902-132,247,079 , GRCh38.p13 chr2: 130,185,329-131,489,506 , PTPN18, 79 more genes
    nsv5220370copy number variation1nstd204human GRCh38.p13 chr2: 131,460,101-131,460,500 , GRCh37.p13 chr2: 132,217,674-132,218,073 RHOQP2
    nsv5219844copy number variation1nstd204human GRCh38.p13 chr2: 131,461,432-131,462,491 , GRCh37.p13 chr2: 132,219,005-132,220,064 RHOQP2
    nsv5217723copy number variation1nstd204human GRCh38.p13 chr2: 131,458,601-131,464,000 , GRCh37.p13 chr2: 132,216,174-132,221,573 RHOQP2
    nsv5217059copy number variation1nstd204human GRCh38.p13 chr2: 131,464,101-131,466,800 , GRCh37.p13 chr2: 132,221,674-132,224,373 RHOQP2
    nsv5216877copy number variation1nstd204human GRCh38.p13 chr2: 131,463,751-131,466,648 , GRCh37.p13 chr2: 132,221,324-132,224,221 RHOQP2
    nsv5216277copy number variation1nstd204human GRCh38.p13 chr2: 131,460,801-131,463,000 , GRCh37.p13 chr2: 132,218,374-132,220,573 RHOQP2
    nsv5206264copy number variation1nstd204human GRCh38.p13 chr2: 131,460,019-131,462,711 , GRCh37.p13 chr2: 132,217,592-132,220,284 RHOQP2
    nsv5206194copy number variation1nstd204human GRCh38.p13 chr2: 131,464,101-131,465,900 , GRCh37.p13 chr2: 132,221,674-132,223,473 RHOQP2
    nsv5037689inversion1nstd200human GRCh38 chr2: 130,226,386-131,459,405 , GRCh37.p13 chr2: 130,983,959-132,216,978 , MTND6P10, 73 more genes
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