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Items: 1 to 20 of 485

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7075901inversion1nstd229human GRCh38 chr15: 99,795,287-101,786,621 , GRCh37.p13 chr15: 100,335,492-102,326,824 GOLGA8VP, DNM1P46, 39 more genes
    nsv7072319inversion1nstd229human GRCh38 chr15: 99,798,704-101,768,404 , GRCh37.p13 chr15: 100,338,909-102,308,607 ADAMTS17, TARS3, 37 more genes
    nsv7067779inversion1nstd229human GRCh38 chr15: 101,562,826-101,789,070 , GRCh37.p13 chr15: 102,103,029-102,329,273 TARS3, GOLGA8VP, 7 more genes
    nsv7059511inversion1nstd229human GRCh38 chr15: 99,784,046-101,789,074 , GRCh37.p13 chr15: 100,324,251-102,329,277 RNA5SP402, TM2D3, 40 more genes
    nsv7059122inversion1nstd229human GRCh38 chr15: 101,611,263-101,625,832 , GRCh37.p13 chr15: 102,151,466-102,166,035 LINC02348
    nsv6977605copy number variation1nstd229human GRCh38 chr15: 101,565,643-101,615,630 , GRCh37.p13 chr15: 102,105,846-102,155,833 LINC02348
    nsv6974884copy number variation1nstd229human GRCh38 chr15: 101,554,931-101,668,829 , GRCh37.p13 chr15: 102,095,134-102,209,032 RNU6-807P, TM2D3, 3 more genes
    nsv6973042copy number variation1nstd229human GRCh38 chr15: 101,127,371-101,697,216 , GRCh37.p13 chr15: 101,667,576-102,237,419 LOC107987228, CHSY1, 12 more genes
    nsv6972925copy number variation1nstd229human GRCh38 chr15: 101,435,713-101,643,288 , GRCh37.p13 chr15: 101,975,918-102,183,491 TM2D3, LINC02348, 3 more genes
    nsv6971844copy number variation1nstd229human GRCh38 chr15: 101,597,301-101,622,100 , GRCh37.p13 chr15: 102,137,504-102,162,303 LINC02348
    nsv6969099copy number variation1nstd229human GRCh38 chr15: 101,550,977-101,638,523 , GRCh37.p13 chr15: 102,091,180-102,178,726 TM2D3, SNRPCP18, 1 more genes
    nsv6968684copy number variation1nstd229human GRCh38 chr15: 101,597,445-101,672,676 , GRCh37.p13 chr15: 102,137,648-102,212,879 TARS3, TM2D3, 2 more genes
    nsv6968044copy number variation1nstd229human GRCh38 chr15: 101,556,104-101,608,521 , GRCh37.p13 chr15: 102,096,307-102,148,724 SNRPCP18, LINC02348
    nsv6967775copy number variation1nstd229human GRCh38 chr15: 101,531,797-101,610,047 , GRCh37.p13 chr15: 102,072,000-102,150,250 SNRPCP18, LINC02348
    nsv6967453copy number variation1nstd229human GRCh38 chr15: 101,405,718-101,610,517 , GRCh37.p13 chr15: 101,945,923-102,150,720 LINC02348, LOC107987228, 2 more genes
    nsv6966074copy number variation1nstd229human GRCh38 chr15: 101,611,301-101,681,900 , GRCh37.p13 chr15: 102,151,504-102,222,103 TARS3, LINC02348, 2 more genes
    nsv6966003copy number variation1nstd229human GRCh38 chr15: 101,486,791-101,773,813 , GRCh37.p13 chr15: 102,026,996-102,314,016 PCSK6, GOLGA8VP, 9 more genes
    nsv6961047copy number variation1nstd229human GRCh38 chr15: 101,495,668-101,682,926 , GRCh37.p13 chr15: 102,035,871-102,223,129 TM2D3, RNU6-807P, 3 more genes
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