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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077330inversion1nstd229human GRCh38 chr21: 20,333,755-29,497,356 , GRCh37.p13 chr21: 21,706,067-30,869,676 LOC105372770, LOC100419737, 95 more genes
    nsv7077119inversion1nstd229human GRCh38 chr21: 21,696,596-22,901,176 , GRCh37.p13 chr21: 23,068,916-24,273,497 LINC00308, LINC01425, 7 more genes
    nsv7075453inversion1nstd229human GRCh38 chr21: 19,130,361-23,504,700 , GRCh37.p13 chr21: 20,502,679-24,877,019 ZNF299P, MIR6130, 34 more genes
    nsv7073324inversion1nstd229human GRCh38 chr21: 20,043,720-24,482,744 , GRCh37.p13 chr21: 21,416,033-25,855,058 KRT18P2, RNU6-772P, 30 more genes
    nsv7069235inversion1nstd229human GRCh38 chr21: 15,814,137-22,638,792 , GRCh37.p13 chr21: 17,186,456-24,011,111 RNU1-98P, CHODL-AS1, 56 more genes
    nsv7068340inversion1nstd229human GRCh38 chr21: 19,574,108-24,248,329 , GRCh37.p13 chr21: 20,946,422-25,620,642 MIR6130, ZNF299P, 34 more genes
    nsv7065993inversion1nstd229human GRCh38 chr21: 15,218,544-21,902,830 , GRCh37.p13 chr21: 16,590,864-23,275,150 LOC107985490, MIR548XHG, 56 more genes
    nsv7065651inversion1nstd229human GRCh38 chr21: 21,109,454-21,737,143 , GRCh37.p13 chr21: 22,481,772-23,109,463 LINC00317, NCAM2
    nsv7037376copy number variation1nstd229human GRCh38 chr21: 21,043,892-24,894,512 , GRCh37.p13 chr21: 22,416,210-26,266,826 RNU4-45P, D21S2088E, 23 more genes
    nsv7037284copy number variation1nstd229human GRCh38 chr21: 21,574,301-21,923,600 , GRCh37.p13 chr21: 22,946,622-23,295,920 LINC01425, LINC00317
    nsv7029923copy number variation1nstd229human GRCh38 chr21: 19,907,468-23,610,014 , GRCh37.p13 chr21: 21,279,782-24,982,332 LINC01687, LINC00320, 26 more genes
    nsv7029078copy number variation1nstd229human GRCh38 chr21: 21,653,500-21,781,280 , GRCh37.p13 chr21: 23,025,821-23,153,600 LINC00317, LINC01425
    nsv7028882copy number variation1nstd229human GRCh38 chr21: 21,235,967-24,018,187 , GRCh37.p13 chr21: 22,608,287-25,390,502 MIR6130, LOC107985512, 20 more genes
    nsv7027840copy number variation1nstd229human GRCh38 chr21: 14,377,890-22,678,900 , GRCh37.p13 chr21: 15,750,211-24,051,220 C1QBPP1, VDAC2P1, 74 more genes
    nsv7027016copy number variation1nstd229human GRCh38 chr21: 21,730,630-21,734,483 , GRCh37.p13 chr21: 23,102,950-23,106,803 LINC00317
    nsv7024315copy number variation1nstd229human GRCh38 chr21: 21,705,501-21,726,600 , GRCh37.p13 chr21: 23,077,821-23,098,920 LINC00317
    nsv7019191copy number variation1nstd229human GRCh38 chr21: 21,670,092-21,723,272 , GRCh37.p13 chr21: 23,042,413-23,095,592 LINC00317
    nsv6637581copy number variation1nstd102humanUncertain significance GRCh37 chr21: 22,789,290-24,987,949 , GRCh38.p12 chr21: 21,416,970-23,615,631 LOC107985512, NCAM2, 17 more genes
    nsv6634469copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,006,457-29,046,428 , GRCh38.p12 chr21: 13,634,136-27,674,109 ADAMTS5, VN2R20P, 160 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
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