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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077186inversion1nstd229human GRCh38 chr15: 35,051,912-40,816,689 , GRCh37.p13 chr15: 35,344,113-41,108,887 BUB1B-PAK6, LOC751603, 96 more genes
    nsv6973151copy number variation1nstd229human GRCh38 chr15: 36,773,702-36,810,546 , GRCh37.p13 chr15: 37,065,903-37,102,747 CDIN1, CSNK1A1P1
    nsv6970245copy number variation1nstd229human GRCh38 chr15: 36,810,147-36,810,342 , GRCh37.p13 chr15: 37,102,348-37,102,543 CSNK1A1P1, CDIN1
    nsv6967512copy number variation1nstd229human GRCh38 chr15: 36,808,708-36,819,915 , GRCh37.p13 chr15: 37,100,909-37,112,116 CDIN1, CSNK1A1P1
    nsv6962400copy number variation1nstd229human GRCh38 chr15: 36,712,416-36,849,479 , GRCh37.p13 chr15: 37,004,617-37,141,680 CSNK1A1P1, CDIN1
    nsv6506357copy number variation1nstd223human GRCh38 chr15: 36,813,601-36,821,000 , GRCh37.p13 chr15: 37,105,802-37,113,201 CSNK1A1P1
    nsv6315190copy number variation1nstd102humanPathogenic GRCh37 chr15: 33,809,650-40,027,263 , GRCh38.p12 chr15: 33,517,449-39,735,062 RYR3, RPL32P2, 84 more genes
    nsv6314189copy number variation1nstd102humanUncertain significance GRCh37 chr15: 36,852,134-37,429,248 , GRCh38.p12 chr15: 36,559,933-37,137,047 MEIS2, TPST2P1, 7 more genes
    nsv6275458copy number variation1nstd214human GRCh38 chr15: 36,800,871-36,800,932 , GRCh37.p13 chr15: 37,093,072-37,093,133 CDIN1, CSNK1A1P1
    nsv6132805copy number variation1nstd213human GRCh37 chr15: 37,040,000-37,550,001 , GRCh38.p12 chr15: 36,747,799-37,257,800 MEIS2, CDIN1, 3 more genes
    nsv6098581insertion1nstd212human GRCh38 chr15: 36,801,908-36,801,908 , GRCh37.p13 chr15: 37,094,109-37,094,109 CSNK1A1P1, CDIN1
    nsv5602767copy number variation1nstd207human GRCh38 chr15: 36,800,871-36,800,932 , GRCh37.p13 chr15: 37,093,072-37,093,133 CDIN1, CSNK1A1P1
    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
    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
    nsv4622786copy number variation1nstd183human GRCh37 chr15: 36,741,975-37,369,170 , GRCh38.p12 chr15: 36,449,774-37,076,969 COX6CP4, TPST2P1, 9 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
    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
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