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Items: 1 to 20 of 136

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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
    nsv6716943copy number variation1nstd229human GRCh38 chr3: 100,336,857-100,342,506 , GRCh37.p13 chr3: 100,055,701-100,061,350 NIT2
    nsv6716278copy number variation1nstd229human GRCh38 chr3: 100,358,201-100,361,600 , GRCh37.p13 chr3: 100,077,045-100,080,444 TOMM70, NIT2
    nsv6715809copy number variation1nstd229human GRCh38 chr3: 100,335,672-100,352,461 , GRCh37.p13 chr3: 100,054,516-100,071,305 NIT2
    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
    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
    nsv6699891copy number variation1nstd229human GRCh38 chr3: 100,355,267-100,358,584 , GRCh37.p13 chr3: 100,074,111-100,077,428 NIT2
    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
    nsv6547764inversion1nstd223human GRCh38 chr3: 100,341,371-100,341,773 , GRCh37.p13 chr3: 100,060,215-100,060,617 NIT2
    nsv6537526inversion1nstd223human GRCh38 chr3: 94,859,299-102,665,887 , GRCh37.p13 chr3: 94,578,143-102,384,731 OR5AC4P, LOC105373996, 112 more genes
    nsv6374426copy number variation1nstd223human GRCh38 chr3: 100,330,701-100,337,800 , GRCh37.p13 chr3: 100,049,545-100,056,644 NIT2
    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
    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
    nsv5904011copy number variation1nstd209human GRCh38 chr3: 100,289,472-100,332,840 , GRCh37.p13 chr3: 100,008,316-100,051,684 NIT2, TBC1D23
    nsv5450858copy number variation1nstd206human GRCh38 chr3: 100,337,655-100,347,383 , GRCh37.p13 chr3: 100,056,499-100,066,227 NIT2
    nsv5040665inversion1nstd200human GRCh38 chr3: 94,638,746-100,409,115 , GRCh37.p13 chr3: 94,357,590-100,127,959 , LOC101929278, 82 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919166copy number variation1nstd200human GRCh38 chr3: 100,336,855-100,342,506 , GRCh37.p13 chr3: 100,055,699-100,061,350 NIT2
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