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Items: 1 to 20 of 222

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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
    nsv7076053inversion1nstd229human GRCh38 chr17: 3,080,168-3,223,685 , GRCh37.p13 chr17: 2,983,462-3,126,979 OR1P1, OR1A2, 5 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
    nsv7065304inversion1nstd229human GRCh38 chr17: 3,155,243-3,316,142 , GRCh37.p13 chr17: 3,058,537-3,219,436 OR1P1, OR3A1, 8 more genes
    nsv7063643inversion1nstd229human GRCh38 chr17: 3,119,267-3,384,121 , GRCh37.p13 chr17: 3,022,561-3,287,415 OR3A1, OR1AC1P, 11 more genes
    nsv6997616copy number variation1nstd229human GRCh38 chr17: 3,146,768-3,253,350 , GRCh37.p13 chr17: 3,050,062-3,156,644 OR1A1, LOC100288728, 3 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
    nsv6995713copy number variation1nstd229human GRCh38 chr17: 3,158,056-3,255,801 , GRCh37.p13 chr17: 3,061,350-3,159,095 OR1D4, OR1A2, 2 more genes
    nsv6992041copy number variation1nstd229human GRCh38 chr17: 3,172,007-3,197,569 , GRCh37.p13 chr17: 3,075,301-3,100,863 LOC100288728, OR1A2
    nsv6988939copy number variation1nstd229human GRCh38 chr17: 3,137,501-3,206,200 , GRCh37.p13 chr17: 3,040,795-3,109,494 OR1P1, LOC100288728, 1 more genes
    nsv6988570copy number variation1nstd229human GRCh38 chr17: 3,157,857-3,207,361 , GRCh37.p13 chr17: 3,061,151-3,110,655 OR1A2, LOC100288728
    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
    nsv6624226copy number variation1nstd224human GRCh37 chr17: 3,049,838-3,482,299 , GRCh38.p12 chr17: 3,146,544-3,579,005 ASPA, OR1A1, 17 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
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