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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7076053inversion1nstd229human GRCh38 chr17: 3,080,168-3,223,685 , GRCh37.p13 chr17: 2,983,462-3,126,979 OR1P1, OR1A2, 5 more genes
    nsv7074857inversion1nstd229human GRCh38 chr17: 3,073,761-3,192,096 , GRCh37.p13 chr17: 2,977,055-3,095,390 OR1G1, LOC100288728, 3 more genes
    nsv7074835inversion1nstd229human GRCh38 chr17: 3,051,093-3,253,100 , GRCh37.p13 chr17: 2,954,387-3,156,394 OR1D2, OR1P1, 7 more genes
    nsv7074630inversion1nstd229human GRCh38 chr17: 1,926,290-3,643,131 , GRCh37.p13 chr17: 1,829,584-3,546,425 SAMD11P1, LOC100288728, 61 more genes
    nsv7074489inversion1nstd229human GRCh38 chr17: 2,996,975-3,267,687 , GRCh37.p13 chr17: 2,900,269-3,170,981 OR1A2, OR1D3P, 9 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7065691inversion1nstd229human GRCh38 chr17: 2,903,074-3,246,959 , GRCh37.p13 chr17: 2,806,368-3,150,253 OR1P1, OR1E3, 9 more genes
    nsv6997498copy number variation1nstd229human GRCh38 chr17: 3,084,469-3,636,714 , GRCh37.p13 chr17: 2,987,763-3,540,008 TRPV1, CTNS, 24 more genes
    nsv6994322copy number variation1nstd229human GRCh38 chr17: 2,881,297-3,104,373 , GRCh37.p13 chr17: 2,784,591-3,007,667 LOC101927911, OR1D5, 2 more genes
    nsv6993931copy number variation1nstd229human GRCh38 chr17: 3,081,105-3,091,451 , GRCh37.p13 chr17: 2,984,399-2,994,745 OR1D2
    nsv6984655copy number variation1nstd229human GRCh38 chr17: 3,088,860-3,098,744 , GRCh37.p13 chr17: 2,992,154-3,002,038 OR1D2
    nsv6984342copy number variation1nstd229human GRCh38 chr17: 3,049,583-3,211,243 , GRCh37.p13 chr17: 2,952,877-3,114,537 OR1G1, LOC100288728, 5 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6637325copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,095,592-3,484,368 , GRCh38.p12 chr17: 1,192,298-3,581,074 SLC43A2, LOC105371592, 81 more genes
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6506401copy number variation1nstd223human GRCh38 chr17: 2,625,215-3,955,354 , GRCh37.p13 chr17: 2,528,509-3,858,648 CLUH, EMC6, 47 more genes
    nsv6503818copy number variation1nstd223human GRCh38 chr17: 3,092,163-3,371,457 , GRCh37.p13 chr17: 2,995,457-3,274,751 OR3A4P, OR1D4, 11 more genes
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