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Items: 1 to 20 of 93

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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
    nsv7142259copy number variation1nstd232human GRCh37.p13 chr17: 26,551,598-26,551,646 , GRCh38.p12 chr17: 28,224,572-28,224,620 PYY2
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6990439copy number variation1nstd229human GRCh38 chr17: 28,226,748-28,226,918 , GRCh37.p13 chr17: 26,553,774-26,553,944 PYY2
    nsv6983931copy number variation1nstd229human GRCh38 chr17: 28,226,498-28,226,575 , GRCh37.p13 chr17: 26,553,524-26,553,601 PYY2
    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
    nsv6190876copy number variation1nstd214human GRCh38 chr17: 28,224,441-28,224,569 , GRCh37.p13 chr17: 26,551,467-26,551,595 PYY2
    nsv6133231copy number variation1nstd213human GRCh37 chr17: 25,820,000-26,720,001 , GRCh38.p12 chr17: 27,492,974-28,392,982 LGALS9, NOS2, 30 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
    nsv6039640copy number variation1nstd212human GRCh38 chr17: 28,224,530-28,224,715 , GRCh37.p13 chr17: 26,551,556-26,551,741 PYY2
    nsv5650784insertion1nstd207human GRCh38 chr17: 28,224,659-28,224,659 , GRCh37.p13 chr17: 26,551,685-26,551,685 PYY2
    nsv5591944copy number variation1nstd207human GRCh38 chr17: 28,224,639-28,224,688 , GRCh37.p13 chr17: 26,551,665-26,551,714 PYY2
    nsv5516080copy number variation1nstd206human GRCh38 chr17: 28,226,748-28,226,925 , GRCh37.p13 chr17: 26,553,774-26,553,951 PYY2
    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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4243070copy number variation1nstd166human GRCh37.p13 chr17: 26,517,014-26,775,312 , GRCh38.p12 chr17: 28,189,988-28,448,294 IFT20, H3P41, 17 more genes
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