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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976101insertion1nstd209human GRCh38 chr15: 36,044,437-36,044,437 , GRCh37.p13 chr15: 36,336,638-36,336,638 LINC02853
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5316435copy number variation1nstd204human GRCh38.p13 chr15: 36,046,096-36,046,224 , GRCh37.p13 chr15: 36,338,297-36,338,425 LINC02853
    nsv5001249copy number variation1nstd200human GRCh38 chr15: 36,046,100-36,046,221 , GRCh37.p13 chr15: 36,338,301-36,338,422 LINC02853
    nsv4855857copy number variation1nstd200human GRCh37 chr15: 36,338,301-36,338,422 , GRCh38.p12 chr15: 36,046,100-36,046,221 LINC02853
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4675391copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053 TPST2P1, AVEN, 65 more genes
    nsv4674936copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-36,861,479 , GRCh38.p12 chr15: 23,319,714-36,569,278 SNORD115-48, MIR4509-2, 330 more genes
    nsv4436396complex substitution1nstd102humanPathogenic GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083 ACTC1, BUB1B, 150 more genes
    nsv4240085copy number variation1nstd166human GRCh37.p13 chr15: 36,306,669-36,345,871 , GRCh38.p12 chr15: 36,014,468-36,053,670 LINC02853
    nsv3935657copy number variation1nstd167human GRCh37 chr15: 36,336,630-36,336,667 , GRCh38.p12 chr15: 36,044,429-36,044,466 LINC02853
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3921026copy number variation1nstd102humanPathogenic NCBI36 chr15: 22,830,109-35,283,797 , GRCh38 chr15: 25,033,869-37,204,304 , GRCh37 chr15: 25,279,016-37,496,505 SNORD116-17, LOC100996670, 303 more genes
    nsv3920384copy number variation1nstd102humanPathogenic NCBI36 chr15: 30,405,629-37,473,561 , GRCh38 chr15: 32,326,136-39,394,068 , GRCh37 chr15: 32,618,337-39,686,269 PGBD4, LOC105370763, 113 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3919055copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,880,216-39,572,605 , NCBI36 chr15: 32,667,508-37,359,897 , GRCh38 chr15: 34,588,015-39,280,404 DPH6, NUTF2P6, 56 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917652copy number variation1nstd102humanPathogenic NCBI36 chr15: 20,249,886-36,169,075 , GRCh38 chr15: 23,319,714-38,089,582 , GRCh37 chr15: 22,698,522-38,381,783 LOC105370764, RN7SL673P, 345 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
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