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Items: 1 to 20 of 122

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5527104copy number variation1nstd206human GRCh38 chr15: 79,925,079-79,925,148 , GRCh37.p13 chr15: 80,217,421-80,217,490 ST20-AS1
    nsv5522730copy number variation1nstd206human GRCh38 chr15: 79,924,533-79,953,030 , GRCh37.p13 chr15: 80,216,875-80,245,372 ST20-AS1, FDPSP9
    nsv5519371copy number variation1nstd206human GRCh38 chr15: 79,898,256-79,960,344 , GRCh37.p13 chr15: 80,190,598-80,252,686 BCL2A1, ST20-AS1, 3 more genes
    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
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4728833copy number variation1nstd102humanUncertain significance GRCh37 chr15: 79,679,772-80,383,301 , GRCh38.p12 chr15: 79,387,430-80,090,959 MTHFS, LOC105370919, 15 more genes
    nsv4632501copy number variation1nstd183human GRCh37 chr15: 80,213,634-80,263,338 , GRCh38.p12 chr15: 79,921,292-79,970,996 ST20-AS1, ST20, 3 more genes
    nsv4631109copy number variation1nstd183human GRCh37 chr15: 79,994,441-80,391,054 , GRCh38.p12 chr15: 79,702,099-80,098,712 RNU6-667P, ST20-AS1, 9 more genes
    nsv4624176copy number variation1nstd183human GRCh37 chr15: 80,172,198-80,247,460 , GRCh38.p12 chr15: 79,879,856-79,955,118 ST20-AS1, ST20, 3 more genes
    nsv4621852copy number variation1nstd183human GRCh37 chr15: 80,190,540-80,252,603 , GRCh38.p12 chr15: 79,898,198-79,960,261 ST20-AS1, FDPSP9, 3 more genes
    nsv4418523copy number variation1nstd174human GRCh37 chr15: 80,190,522-80,252,791 , GRCh38.p12 chr15: 79,898,180-79,960,449 ST20-AS1, FDPSP9, 3 more genes
    nsv4249349copy number variation1nstd166human GRCh37.p13 chr15: 80,216,875-80,245,435 , GRCh38.p12 chr15: 79,924,533-79,953,093 ST20-AS1, FDPSP9
    nsv4246777copy number variation1nstd166human GRCh37.p13 chr15: 80,217,421-80,217,490 , GRCh38.p12 chr15: 79,925,079-79,925,148 ST20-AS1
    nsv4245057copy number variation1nstd166human GRCh37.p13 chr15: 80,216,148-80,223,605 , GRCh38.p12 chr15: 79,923,806-79,931,263 ST20, ST20-AS1
    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
    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
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 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
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