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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947392copy number variation1nstd209human GRCh38 chr15: 71,816,503-71,817,321 , GRCh37.p13 chr15: 72,108,844-72,109,662 NR2E3
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5672588copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,103,074-72,110,035 , GRCh38.p12 chr15: 71,810,734-71,817,694 NR2E3
    nsv5528530copy number variation1nstd206human GRCh38 chr15: 71,816,361-71,817,199 , GRCh37.p13 chr15: 72,108,702-72,109,540 NR2E3
    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
    nsv5005561copy number variation1nstd200human GRCh38 chr15: 71,816,376-71,817,308 , GRCh37.p13 chr15: 72,108,717-72,109,649 NR2E3
    nsv4863877copy number variation1nstd200human GRCh37 chr15: 72,108,708-72,109,659 , GRCh38.p12 chr15: 71,816,367-71,817,318 NR2E3
    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
    nsv4703626copy number variation1nstd195human GRCh37 chr15: 72,105,901-72,199,201 , GRCh38.p12 chr15: 71,813,561-71,906,860 MYO9A, NR2E3, 1 more genes
    nsv4634108copy number variation1nstd183human GRCh37 chr15: 71,945,010-72,272,867 , GRCh38.p12 chr15: 71,652,671-71,980,526 MYO9A, NR2E3, 4 more genes
    nsv4622384copy number variation1nstd183human GRCh37 chr15: 72,104,070-72,105,911 , GRCh38.p12 chr15: 71,811,730-71,813,571 NR2E3
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
    nsv4251184copy number variation1nstd166human GRCh37.p13 chr15: 72,108,727-72,109,603 , GRCh38.p12 chr15: 71,816,386-71,817,262 NR2E3
    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
    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
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 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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