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Items: 1 to 20 of 188

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961185insertion1nstd209human GRCh38 chr2: 96,499,868-96,499,868 , GRCh37.p13 chr2: 97,165,605-97,165,605 NEURL3
    nsv5876678copy number variation1nstd209human GRCh38 chr2: 95,981,467-97,579,646 , GRCh37.p13 chr2: 96,647,215-98,196,109 , ARID5A, 48 more genes
    nsv5875852copy number variation1nstd209human GRCh38 chr2: 96,452,841-96,507,955 , GRCh37.p13 chr2: 97,118,578-97,173,692 NEURL3
    nsv5834213copy number variation1nstd209human GRCh38 chr2: 96,500,125-96,501,924 , GRCh37.p13 chr2: 97,165,862-97,167,661 NEURL3
    nsv5834212copy number variation1nstd209human GRCh38 chr2: 96,452,925-96,507,984 , GRCh37.p13 chr2: 97,118,662-97,173,721 NEURL3
    nsv5715612mobile element insertion2nstd211human GRCh38 chr2: 96,499,882-96,499,882 , GRCh37.p13 chr2: 97,165,619-97,165,619 NEURL3
    nsv5677910mobile element insertion1nstd211human GRCh38 chr2: 96,499,882-96,499,882 , GRCh37.p13 chr2: 97,165,619-97,165,619 NEURL3
    nsv5617774insertion1nstd207human GRCh38 chr2: 96,499,868-96,499,868 , GRCh37.p13 chr2: 97,165,605-97,165,605 NEURL3
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5403954mobile element insertion1nstd206human GRCh38 chr2: 96,499,882-96,499,927 , GRCh37.p13 chr2: 97,165,619-97,165,664 NEURL3
    nsv5381491copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,755,045-98,021,592 , GRCh38.p12 chr2: 96,089,297-97,285,797 LOC100421288, STARD7, 34 more genes
    nsv5381324copy number variation1nstd102humanPathogenic GRCh37 chr2: 96,737,083-98,193,473 , GRCh38.p12 chr2: 96,071,335-97,577,010 IGKV2OR2-8, LOC100506076, 42 more genes
    nsv5215020copy number variation1nstd204human GRCh38.p13 chr2: 96,060,101-97,188,600 , GRCh37.p13 chr2: 96,725,849-97,854,337 RN7SL313P, NCAPH, 33 more genes
    nsv5199588mobile element insertion1nstd203human GRCh38 chr2: 96,499,868-96,499,882 , GRCh37.p13 chr2: 97,165,605-97,165,619 NEURL3
    nsv5185072mobile element insertion1nstd203human GRCh38 chr2: 96,499,875-96,499,882 , GRCh37.p13 chr2: 97,165,612-97,165,619 NEURL3
    nsv5183487mobile element insertion1nstd203human GRCh38 chr2: 96,499,873-96,499,882 , GRCh37.p13 chr2: 97,165,610-97,165,619 NEURL3
    nsv5180324mobile element insertion1nstd203human GRCh38 chr2: 96,499,872-96,499,882 , GRCh37.p13 chr2: 97,165,609-97,165,619 NEURL3
    nsv5067592mobile element insertion1nstd203human GRCh38 chr2: 96,499,125-96,499,136 , GRCh37.p13 chr2: 97,164,862-97,164,873 NEURL3
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
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