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Items: 1 to 20 of 632

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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
    nsv7146297copy number variation1nstd232human GRCh37.p13 chr17: 673,194-673,281 , GRCh38.p12 chr17: 769,954-770,041 GLOD4
    nsv7140754insertion1nstd232human GRCh37.p13 chr17: 671,941-671,941 , GRCh38.p12 chr17: 768,701-768,701 GLOD4
    nsv7137132copy number variation1nstd102humanUncertain significance GRCh37 chr17: 65,445-695,309 , GRCh38.p12 chr17: 215,654-792,069 RPS4XP17, RFLNB, 11 more genes
    nsv7098743copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802 PAFAH1B1, RN7SL33P, 65 more genes
    nsv7098729copy number variation1nstd102humanPathogenic GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857 MYO1C, SERPINF1, 42 more genes
    nsv7094905copy number variation1nstd102humanUncertain significance GRCh37 chr17: 505,015-722,805 , GRCh38.p12 chr17: 601,775-819,565 , GRCh38.p12 chr17|NW_017363817.1: 161,252-281,919 GLOD4, TLCD3A, 6 more genes
    nsv7094896copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446 SLC43A2, LOC105371480, 34 more genes
    nsv7077982inversion1nstd229human GRCh38 chr17: 662,447-915,193 , GRCh37.p13 chr17: 565,687-818,433 GLOD4, LOC101927727, 6 more genes
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7077460inversion1nstd229human GRCh38 chr17: 659,158-885,293 , GRCh37.p13 chr17: 562,398-788,533 TLCD3A, DBIL5P, 5 more genes
    nsv7070618inversion1nstd229human GRCh38 chr17: 426,050-796,506 , GRCh37.p13 chr17: 396,627-699,746 GEMIN4, MRM3, 6 more genes
    nsv7060051inversion1nstd229human GRCh38 chr17: 689,006-865,724 , GRCh37.p13 chr17: 592,246-768,964 MRM3, VPS53, 5 more genes
    nsv6997881copy number variation1nstd229human GRCh38 chr17: 702,538-793,182 , GRCh37.p13 chr17: 605,778-696,422 MRM3, VPS53, 4 more genes
    nsv6997420copy number variation1nstd229human GRCh38 chr17: 768,742-774,538 , GRCh37.p13 chr17: 671,982-677,778 GLOD4
    nsv6995935copy number variation1nstd229human GRCh38 chr17: 764,800-765,552 , GRCh37.p13 chr17: 668,040-668,792 GLOD4
    nsv6995849copy number variation1nstd229human GRCh38 chr17: 426,628-969,586 , GRCh37.p13 chr17: 396,627-872,826 VPS53, MRM3, 8 more genes
    nsv6995290copy number variation1nstd229human GRCh38 chr17: 785,566-785,913 , GRCh37.p13 chr17: 688,806-689,153 MRM3, GLOD4
    nsv6994274copy number variation1nstd229human GRCh38 chr17: 779,326-798,247 , GRCh37.p13 chr17: 682,566-701,487 MRM3, GLOD4, 1 more genes
    nsv6991988copy number variation1nstd229human GRCh38 chr17: 251,815-1,065,942 , GRCh37.p13 chr17: 396,627-969,182 LIAT1, RPS4XP17, 17 more genes
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