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Items: 1 to 20 of 76

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv4231925copy number variation1nstd166human GRCh37.p13 chr12: 112,038,413-112,386,197 , GRCh38.p12 chr12: 111,600,609-111,948,393 MAPKAPK5, BRAP, 10 more genes
    nsv3916234copy number variation1nstd102humanPathogenic NCBI36 chr12: 104,152,585-111,116,873 , GRCh37 chr12: 105,628,455-112,632,490 , GRCh38 chr12: 105,234,677-112,194,686 LOC100287944, PWP1, 141 more genes
    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
    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
    nsv3897722copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059 , RNU4ATAC16P, 2452 more genes
    nsv3169098inversion1nstd158human GRCh37 chr12: 28,095,967-121,612,723 , GRCh38.p12 chr12: 27,943,034-121,174,920 , ACACB, 1642 more genes
    nsv3168340inversion1nstd158human GRCh37 chr12: 66,451,836-123,782,201 , GRCh38.p12 chr12: 66,058,056-123,297,654 , ACACB, 909 more genes
    nsv3153548copy number variation1nstd151human GRCh37 chr12: 112,305,374-112,381,176 , GRCh38.p12 chr12: 111,867,570-111,943,372 ADAM1A, ADAM1B, 3 more genes
    nsv2786288copy number variation1nstd132human NCBI36 chr12: 110,529,335-110,928,343 , GRCh37.p13 chr12: 112,044,952-112,443,960 , GRCh38.p12 chr12: 111,607,148-112,006,156 TMEM116, LOC724085, 11 more genes
    nsv2783944copy number variation1nstd132human NCBI36 chr12: 110,220,461-111,002,025 , GRCh37.p13 chr12: 111,736,078-112,517,642 , GRCh38.p12 chr12: 111,298,274-112,079,838 ERP29, CUX2, 25 more genes
    nsv2768213copy-neutral loss of heterozygosity1nstd125human GRCh38.p12 chr12: 109,335,169-113,005,376 , GRCh37 chr12: 109,772,974-113,443,181 ALDH2, ATP2A2, 80 more genes
    nsv2740531copy number variation1nstd130human NCBI36 chr12: 49,559,698-128,874,436 , GRCh37.p13 chr12: 51,273,431-130,308,483 , GRCh38.p12 chr12: 50,879,648-129,823,938 , LINC01234, 1477 more genes
    nsv2739875copy number variation1nstd130human NCBI36 chr12: 83,709,527-131,568,361 , GRCh37.p13 chr12: 85,185,396-133,058,288 , GRCh38.p12 chr12: 84,791,617-132,481,702 , POC1B-GALNT4, 863 more genes
    nsv2735999copy number variation1nstd130human NCBI36 chr12: 64,079-132,288,869 , GRCh37.p13 chr12: 282,465-133,778,796 , GRCh38.p12 chr12: 84,652-133,202,210 , CHST11, 2525 more genes
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