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Items: 1 to 20 of 298

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5730520mobile element insertion2nstd211human GRCh38 chr2: 110,666,693-110,666,693 , GRCh37.p13 chr2: 111,424,270-111,424,270 BUB1
    nsv5680359mobile element insertion1nstd211human GRCh38 chr2: 110,644,058-110,644,058 , GRCh37.p13 chr2: 111,401,635-111,401,635 BUB1
    nsv5680275mobile element insertion1nstd211human GRCh38 chr2: 110,644,081-110,644,081 , GRCh37.p13 chr2: 111,401,658-111,401,658 BUB1
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5555398mobile element insertion1nstd206human GRCh38 chr2: 110,666,693-110,666,744 , GRCh37.p13 chr2: 111,424,270-111,424,321 BUB1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449197copy number variation1nstd206human GRCh38 chr2: 110,662,648-110,663,847 , GRCh37.p13 chr2: 111,420,225-111,421,424 BUB1
    nsv5435509copy number variation1nstd206human GRCh38 chr2: 109,743,550-110,910,000 , GRCh37.p13 chr2: 110,501,127-111,667,577 MIR4436B2, LOC112268438, 40 more genes
    nsv5204819copy number variation1nstd204human GRCh38.p13 chr2: 110,612,832-110,664,446 , GRCh37.p13 chr2: 111,370,409-111,422,023 LOC105373553, RPL22P12, 2 more genes
    nsv5200281copy number variation1nstd102humanUncertain significance GRCh37 chr2: 110,833,650-111,406,694 , GRCh38.p12 chr2: 110,076,073-110,649,117 LINC01106, LIMS4, 20 more genes
    nsv5077043mobile element insertion1nstd203human GRCh38 chr2: 110,662,943-110,662,959 , GRCh37.p13 chr2: 111,420,520-111,420,536 BUB1
    nsv5068300mobile element insertion1nstd203human GRCh38 chr2: 110,644,058-110,644,081 , GRCh37.p13 chr2: 111,401,635-111,401,658 BUB1
    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
    nsv4915009copy number variation1nstd200human GRCh38 chr2: 110,662,647-110,663,848 , GRCh37.p13 chr2: 111,420,224-111,421,425 BUB1
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 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
    nsv4765126inversion1nstd199human GRCh37 chr2: 109,141,438-113,110,493 , GRCh38.p12 chr2: 108,524,982-112,352,916 , BUB1, 92 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
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