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Items: 1 to 20 of 306

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139704insertion1nstd232human GRCh37.p13 chr5: 180,222,941-180,222,941 , GRCh38.p12 chr5: 180,795,941-180,795,941 MGAT1
    nsv7053423inversion1nstd229human GRCh38 chr5: 180,767,059-181,141,901 , GRCh37.p13 chr5: 180,194,059-180,568,901 HEIH, TRV-CAC1-3, 19 more genes
    nsv7045576inversion1nstd229human GRCh38 chr5: 180,805,627-181,281,045 , GRCh37.p13 chr5: 180,232,627-180,708,046 RPL13P10, TRV-AAC1-3, 46 more genes
    nsv6797376copy number variation1nstd229human GRCh38 chr5: 180,783,904-180,788,968 , GRCh37.p13 chr5: 180,210,904-180,215,968 MGAT1
    nsv6795355copy number variation1nstd229human GRCh38 chr5: 180,800,901-180,816,400 , GRCh37.p13 chr5: 180,227,901-180,243,400 MGAT1
    nsv6795222copy number variation1nstd229human GRCh38 chr5: 180,785,301-180,861,900 , GRCh37.p13 chr5: 180,212,301-180,288,900 ZFP62, LINC00847, 2 more genes
    nsv6794678copy number variation1nstd229human GRCh38 chr5: 180,793,099-180,808,645 , GRCh37.p13 chr5: 180,220,099-180,235,645 MGAT1
    nsv6794354copy number variation1nstd229human GRCh38 chr5: 180,767,201-180,890,800 , GRCh37.p13 chr5: 180,194,201-180,317,800 HEIH, ZFP62, 2 more genes
    nsv6792842copy number variation1nstd229human GRCh38 chr5: 180,797,795-180,797,851 , GRCh37.p13 chr5: 180,224,795-180,224,851 MGAT1
    nsv6791692copy number variation1nstd229human GRCh38 chr5: 180,685,035-180,786,372 , GRCh37.p13 chr5: 180,112,035-180,213,372 RNU1-17P, OR2Y1, 3 more genes
    nsv6791281copy number variation1nstd229human GRCh38 chr5: 180,572,466-180,861,055 , GRCh37.p13 chr5: 179,999,466-180,288,055 MGAT1, OR2Y1, 10 more genes
    nsv6788052copy number variation1nstd229human GRCh38 chr5: 180,788,119-180,788,163 , GRCh37.p13 chr5: 180,215,119-180,215,163 MGAT1
    nsv6787957copy number variation1nstd229human GRCh38 chr5: 180,684,834-180,791,724 , GRCh37.p13 chr5: 180,111,834-180,218,724 OR2Y1, MGAT1, 3 more genes
    nsv6785852copy number variation1nstd229human GRCh38 chr5: 180,805,238-180,805,269 , GRCh37.p13 chr5: 180,232,238-180,232,269 MGAT1
    nsv6783769copy number variation1nstd229human GRCh38 chr5: 180,522,158-180,793,884 , GRCh37.p13 chr5: 179,949,158-180,220,884 OR2Y1, MGAT1, 8 more genes
    nsv6783570copy number variation1nstd229human GRCh38 chr5: 180,766,236-180,791,374 , GRCh37.p13 chr5: 180,193,236-180,218,374 MGAT1
    nsv6780298copy number variation1nstd229human GRCh38 chr5: 180,811,506-180,818,171 , GRCh37.p13 chr5: 180,238,506-180,245,171 MGAT1
    nsv6779431copy number variation1nstd229human GRCh38 chr5: 180,757,199-180,788,064 , GRCh37.p13 chr5: 180,184,199-180,215,064 MGAT1
    nsv6636938copy number variation1nstd102humanUncertain significance GRCh37 chr5: 179,922,498-180,608,605 , GRCh38.p12 chr5: 180,495,498-181,181,605 RNU6-1036P, TRL-AAG7-1, 34 more genes
    nsv6636455copy number variation1nstd102humanUncertain significance GRCh37 chr5: 180,148,276-180,719,789 , GRCh38.p12 chr5: 180,721,276-181,292,788 OR2Y1, TRV-AAC1-2, 48 more genes
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