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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5667399inversion1nstd207human GRCh38 chr2: 108,527,822-109,733,036 , GRCh37.p13 chr2: 109,144,278-110,490,613 , LIMS1, 20 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
    nsv5434507copy number variation1nstd206human GRCh38 chr2: 109,589,618-109,812,809 , GRCh37.p13 chr2: 110,347,195-110,570,386 SOWAHC, RGPD5, 7 more genes
    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
    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
    nsv4728410copy number variation1nstd102humanPathogenic GRCh37 chr2: 107,029,680-113,187,742 , GRCh38.p12 chr2: 106,413,224-112,430,165 RPL10P5, BUB1, 121 more genes
    nsv4674320copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 108,499,809-110,504,318 , GRCh38.p12 chr2: 107,883,353-109,746,741 LIMS1, RANBP2, 37 more genes
    nsv4582150copy number variation1nstd183human GRCh37 chr2: 110,367,969-110,504,346 , GRCh38.p12 chr2: 109,610,392-109,746,769 SOWAHC, SEPTIN10, 5 more genes
    nsv4582149copy number variation1nstd183human GRCh37 chr2: 110,366,819-110,584,070 , GRCh38.p12 chr2: 109,609,242-109,826,493 SOWAHC, RGPD5, 7 more genes
    nsv4410174copy number variation1nstd174human GRCh37 chr2: 110,348,959-110,462,496 , GRCh38.p12 chr2: 109,591,382-109,704,919 SOWAHC, LOC105373545, 2 more genes
    nsv4408139copy number variation1nstd174human GRCh37 chr2: 110,261,667-111,400,650 , GRCh38.p12 chr2: 109,504,090-110,643,073 , SOWAHC, 47 more genes
    nsv4386981copy number variation1nstd173human GRCh37 chr2: 110,349,132-110,504,330 , GRCh38.p12 chr2: 109,591,555-109,746,753 SOWAHC, LOC107985774, 5 more genes
    nsv4380516copy number variation1nstd173human GRCh37 chr2: 110,376,135-110,448,923 , GRCh38.p12 chr2: 109,618,558-109,691,346 SOWAHC, BMS1P19
    nsv4376435copy number variation1nstd173human GRCh37 chr2: 110,273,611-111,365,996 , GRCh38.p12 chr2: 109,516,034-110,608,419 , LIMS4, 43 more genes
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