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Items: 1 to 20 of 551

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7137114copy number variation1nstd102humanPathogenic GRCh37 chr15: 98,996,113-101,211,899 , GRCh38.p12 chr15: 98,452,884-100,671,694 PGPEP1L, LOC105371017, 36 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv7074837inversion1nstd229human GRCh38 chr15: 98,618,777-101,109,346 , GRCh37.p13 chr15: 99,162,006-101,649,551 LOC440313, PRKXP1, 42 more genes
    nsv7065226inversion1nstd229human GRCh38 chr15: 98,338,625-100,843,802 , GRCh37.p13 chr15: 98,881,854-101,384,007 LOC102723335, LUNAR1, 39 more genes
    nsv7064824inversion1nstd229human GRCh38 chr15: 98,981,210-99,387,289 , GRCh37.p13 chr15: 99,524,439-99,927,494 SYNM-AS1, TTC23, 6 more genes
    nsv7064682inversion1nstd229human GRCh38 chr15: 99,334,911-100,692,064 , GRCh37.p13 chr15: 99,875,116-101,232,269 LOC400464, LOC105371020, 24 more genes
    nsv7064311inversion1nstd229human GRCh38 chr15: 99,320,520-99,873,567 , GRCh37.p13 chr15: 99,860,725-100,413,772 LYSMD4, LRRC28, 10 more genes
    nsv7063694inversion1nstd229human GRCh38 chr15: 98,738,473-100,284,229 , GRCh37.p13 chr15: 99,281,702-100,824,434 MIR4714, PGPEP1L, 22 more genes
    nsv7058435inversion1nstd229human GRCh38 chr15: 99,189,235-99,257,521 , GRCh37.p13 chr15: 99,729,440-99,797,726 HSP90B2P, TTC23, 1 more genes
    nsv6977420copy number variation1nstd229human GRCh38 chr15: 99,228,901-99,260,000 , GRCh37.p13 chr15: 99,769,106-99,800,205 HSP90B2P, LRRC28, 1 more genes
    nsv6977137copy number variation1nstd229human GRCh38 chr15: 98,919,969-99,497,854 , GRCh37.p13 chr15: 99,463,198-100,038,059 SYNM, LINC02244, 11 more genes
    nsv6976840copy number variation1nstd229human GRCh38 chr15: 99,204,704-99,306,705 , GRCh37.p13 chr15: 99,744,909-99,846,910 HNRNPA1P62, TTC23, 2 more genes
    nsv6976088copy number variation1nstd229human GRCh38 chr15: 99,379,352-99,432,621 , GRCh37.p13 chr15: 99,919,557-99,972,826 LINC02244, LRRC28, 1 more genes
    nsv6976076copy number variation1nstd229human GRCh38 chr15: 99,269,372-99,318,159 , GRCh37.p13 chr15: 99,809,577-99,858,364 HNRNPA1P62, LRRC28
    nsv6975448copy number variation1nstd229human GRCh38 chr15: 99,287,678-99,287,776 , GRCh37.p13 chr15: 99,827,883-99,827,981 LRRC28
    nsv6975140copy number variation1nstd229human GRCh38 chr15: 99,340,554-99,342,385 , GRCh37.p13 chr15: 99,880,759-99,882,590 LRRC28
    nsv6974887copy number variation1nstd229human GRCh38 chr15: 99,281,419-99,281,497 , GRCh37.p13 chr15: 99,821,624-99,821,702 LRRC28
    nsv6973736copy number variation1nstd229human GRCh38 chr15: 99,303,815-99,304,140 , GRCh37.p13 chr15: 99,844,020-99,844,345 LRRC28
    nsv6973134copy number variation1nstd229human GRCh38 chr15: 99,385,290-99,463,577 , GRCh37.p13 chr15: 99,925,495-100,003,782 LOC105371017, LINC02244, 1 more genes
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