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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7094786copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,636,418-73,660,611 , GRCh38.p12 chr15: 72,344,077-73,368,270 LOC105370890, HIGD2B, 24 more genes
    nsv7094632copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,847,592-73,660,611 , GRCh38.p12 chr15: 72,555,251-73,368,270 MIR630, LINC02259, 18 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6961204copy number variation1nstd229human GRCh38 chr15: 72,540,230-73,128,775 , GRCh37.p13 chr15: 72,832,571-73,421,116 LOC112268145, LOC107984801, 13 more genes
    nsv6309803copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,103,084-74,244,178 , GRCh38.p12 chr15: 71,810,744-73,951,837 PHB1P20, TMEM202, 51 more genes
    nsv6133155copy number variation1nstd213human GRCh37 chr15: 72,730,000-102,440,001 , GRCh38.p12 chr15: 72,437,659-101,899,798 , BLM, 609 more genes
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    nsv6132908copy number variation1nstd213human GRCh37 chr15: 72,860,000-75,530,001 , GRCh38.p12 chr15: 72,567,659-75,237,660 BBS4, CYP1A1, 77 more genes
    nsv6132816copy number variation1nstd213human GRCh37 chr15: 72,870,000-73,060,001 , GRCh38.p12 chr15: 72,577,659-72,767,660 BBS4, ARIH1, 9 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
    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
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4683941copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,646,022-73,660,621 , GRCh38.p12 chr15: 72,353,681-73,368,280 TMEM202, PHB1P20, 24 more genes
    nsv4456455copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,825,914-73,067,234 , GRCh38.p12 chr15: 72,533,573-72,774,893 ARIH1, MIR630, 9 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
    nsv3920633copy number variation1nstd102humanPathogenic GRCh38 chr15: 68,830,574-73,823,337 , NCBI36 chr15: 66,909,967-71,902,731 , GRCh37 chr15: 69,122,913-74,115,678 NEO1, LOC390600, 95 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
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