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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv6624216copy number variation1nstd224human GRCh37 chr17: 25,319,272-25,909,816 , GRCh38.p12 chr17: 26,992,246-27,582,790 TBC1D3P5, RPS16P8, 13 more genes
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6291821copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,439,781-26,267,997 , GRCh38.p12 chr17: 27,112,755-27,940,971 ITM2BP1, CPDP1, 17 more genes
    nsv6272080copy number variation1nstd214human GRCh38 chr17: 27,293,215-27,293,267 , GRCh37.p13 chr17: 25,620,241-25,620,293 WSB1, MIR4522
    nsv6133230copy number variation1nstd213human GRCh37 chr17: 25,640,000-25,730,001 , GRCh38.p12 chr17: 27,312,974-27,402,975 WSB1, SYPL1P2, 1 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv5695252mobile element insertion1nstd211human GRCh38 chr17: 27,311,659-27,311,659 , GRCh37.p13 chr17: 25,638,685-25,638,685 WSB1
    nsv5358768translocation1nstd200human GRCh38 chr17: 27,288,934-27,288,934 , GRCh38 chr17: 27,293,316-27,293,316 , GRCh37.p13 chr17: 25,620,342-25,620,342 , GRCh37.p13 chr17: 25,615,960-25,615,960 WSB1, MIR4522
    nsv5329681translocation1nstd200human GRCh37 chr17: 25,620,342-25,620,342 , GRCh37 chr17: 25,615,960-25,615,960 , GRCh38.p12 chr17: 27,293,316-27,293,316 , GRCh38.p12 chr17: 27,288,934-27,288,934 MIR4522, WSB1
    nsv5010199copy number variation1nstd200human GRCh38 chr17: 27,309,559-27,313,772 , GRCh37.p13 chr17: 25,636,585-25,640,798 WSB1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 more genes
    nsv4376928copy number variation1nstd173human GRCh37 chr17: 25,443,376-26,031,625 , GRCh38.p12 chr17: 27,116,350-27,704,599 NOS2P1, KSR1, 13 more genes
    nsv4369372copy number variation1nstd173human GRCh37 chr17: 25,599,639-25,630,989 , GRCh38.p12 chr17: 27,272,613-27,303,963 RPS16P8, WSB1, 2 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4247959copy number variation1nstd166human GRCh37.p13 chr17: 25,617,162-25,666,343 , GRCh38.p12 chr17: 27,290,136-27,339,317 MIR4522, WSB1
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