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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930153copy number variation1nstd209human GRCh38 chr12: 114,589,236-114,589,323 , GRCh37.p13 chr12: 115,027,041-115,027,128 OSTF1P1
    nsv5505039copy number variation1nstd206human GRCh38 chr12: 114,586,939-114,610,914 , GRCh37.p13 chr12: 115,024,744-115,048,719 OSTF1P1
    nsv5504334copy number variation1nstd206human GRCh38 chr12: 114,589,236-114,589,324 , GRCh37.p13 chr12: 115,027,041-115,027,129 OSTF1P1
    nsv4993712copy number variation1nstd200human GRCh38 chr12: 114,584,388-114,590,975 , GRCh37.p13 chr12: 115,022,193-115,028,780 OSTF1P1
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4754840inversion1nstd199human GRCh37 chr12: 104,382,539-125,801,164 , GRCh38.p12 chr12: 103,988,761-125,316,618 , ACACB, 452 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4529773copy number variation1nstd166human GRCh37.p13 chr12: 115,027,041-115,027,129 , GRCh38.p12 chr12: 114,589,236-114,589,324 OSTF1P1
    nsv4508583mobile element insertion1nstd166human GRCh37.p13 chr12: 115,024,441-115,024,441 , GRCh38.p12 chr12: 114,586,636-114,586,636 OSTF1P1
    nsv4218415copy number variation1nstd166human GRCh37.p13 chr12: 115,024,736-115,048,719 , GRCh38.p12 chr12: 114,586,931-114,610,914 OSTF1P1
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
    nsv3913894copy number variation1nstd102humanPathogenic NCBI36 chr12: 113,190,591-132,287,975 , GRCh38 chr12: 114,268,403-133,201,316 , GRCh37 chr12: 114,706,208-133,777,902 TAOK3, LINC02405, 386 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
    nsv3904719copy number variation1nstd102humanPathogenic GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532 , OR5BT1P, 2441 more genes
    nsv3904242copy number variation1nstd102humanPathogenic GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309 , RNA5SP369, 2454 more genes
    nsv3898489copy number variation1nstd102humanUncertain significance GRCh37 chr12: 114,948,986-115,167,687 , GRCh38.p12 chr12: 114,511,181-114,729,882 OSTF1P1, TBX3-AS1, 1 more genes
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
    nsv3890891copy number variation1nstd102humanPathogenic GRCh37 chr12: 114,995,645-115,376,925 , GRCh38.p12 chr12: 114,557,840-114,939,120 TBX3, OSTF1P1, 2 more genes
    nsv3169098inversion1nstd158human GRCh37 chr12: 28,095,967-121,612,723 , GRCh38.p12 chr12: 27,943,034-121,174,920 , ACACB, 1642 more genes
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