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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv6717215copy number variation1nstd229human GRCh38 chr3: 100,387,298-100,391,971 , GRCh37.p13 chr3: 100,106,142-100,110,815 TOMM70
    nsv6716278copy number variation1nstd229human GRCh38 chr3: 100,358,201-100,361,600 , GRCh37.p13 chr3: 100,077,045-100,080,444 TOMM70, NIT2
    nsv6714720copy number variation1nstd229human GRCh38 chr3: 100,389,211-100,416,558 , GRCh37.p13 chr3: 100,108,055-100,135,402 TOMM70, LNP1
    nsv6711446copy number variation1nstd229human GRCh38 chr3: 100,368,987-100,369,045 , GRCh37.p13 chr3: 100,087,831-100,087,889 TOMM70
    nsv6711254copy number variation1nstd229human GRCh38 chr3: 100,305,678-100,378,139 , GRCh37.p13 chr3: 100,024,522-100,096,983 TBC1D23, TOMM70, 1 more genes
    nsv6709454copy number variation1nstd229human GRCh38 chr3: 100,366,701-100,372,400 , GRCh37.p13 chr3: 100,085,545-100,091,244 TOMM70
    nsv6707141copy number variation1nstd229human GRCh38 chr3: 100,293,801-100,412,507 , GRCh37.p13 chr3: 100,012,645-100,131,351 LNP1, NIT2, 2 more genes
    nsv6706465copy number variation1nstd229human GRCh38 chr3: 100,188,066-100,400,094 , GRCh37.p13 chr3: 99,906,910-100,118,938 TBC1D23, VTI1BP1, 5 more genes
    nsv6706454copy number variation1nstd229human GRCh38 chr3: 100,384,159-100,445,738 , GRCh37.p13 chr3: 100,103,003-100,164,582 LNP1, TOMM70
    nsv6628611copy number variation1nstd224human GRCh37 chr3: 100,000,682-100,321,689 , GRCh38.p12 chr3: 100,281,838-100,602,845 TOMM70, TBC1D23, 3 more genes
    nsv6551404inversion1nstd223human GRCh38 chr3: 100,379,552-100,379,748 , GRCh37.p13 chr3: 100,098,396-100,098,592 TOMM70
    nsv6540764inversion1nstd223human GRCh38 chr3: 100,392,424-100,393,180 , GRCh37.p13 chr3: 100,111,268-100,112,024 TOMM70
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6361598copy number variation1nstd223human GRCh38 chr3: 100,398,190-100,399,149 , GRCh37.p13 chr3: 100,117,034-100,117,993 TOMM70
    nsv6359248copy number variation1nstd223human GRCh38 chr3: 100,378,101-100,380,100 , GRCh37.p13 chr3: 100,096,945-100,098,944 TOMM70
    nsv6357476copy number variation1nstd223human GRCh38 chr3: 100,305,678-100,378,133 , GRCh37.p13 chr3: 100,024,522-100,096,977 TOMM70, TBC1D23, 1 more genes
    nsv6254403mobile element insertion1nstd215human GRCh38 chr3: 100,393,687-100,393,687 , GRCh37.p13 chr3: 100,112,531-100,112,531 TOMM70
    nsv6166875copy number variation1nstd214human GRCh38 chr3: 100,365,791-100,365,849 , GRCh37.p13 chr3: 100,084,635-100,084,693 TOMM70
    nsv6134718copy number variation1nstd213human GRCh37 chr3: 99,980,000-100,190,001 , GRCh38.p12 chr3: 100,261,156-100,471,157 TOMM70, TBC1D23, 2 more genes
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