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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
    nsv4530392copy number variation1nstd166human GRCh37.p13 chr12: 113,714,000-113,739,000 , GRCh38.p12 chr12: 113,276,195-113,301,195 , TPCN1, 2 more genes
    nsv4456436copy number variation1nstd102humanUncertain significance GRCh37 chr12: 113,695,889-113,904,780 , GRCh38.p12 chr12: 113,258,084-113,466,975 SDSL, TPCN1, 6 more genes
    nsv4380311copy number variation1nstd173human GRCh37 chr12: 113,628,648-113,905,101 , GRCh38.p12 chr12: 113,190,843-113,467,296 , IQCD, 9 more genes
    nsv4374351copy number variation1nstd173human GRCh37 chr12: 113,630,747-113,904,780 , GRCh38.p12 chr12: 113,192,942-113,466,975 , SLC8B1, 8 more genes
    nsv4365342copy number variation2nstd173human GRCh37 chr12: 113,628,648-113,923,854 , GRCh38.p12 chr12: 113,190,843-113,486,049 , SDS, 10 more genes
    nsv4342640sequence alteration1nstd166human GRCh37.p13 chr12: 113,723,986-113,737,287 , GRCh38.p12 chr12: 113,286,181-113,299,482 , TPCN1, 2 more genes
    nsv4221722copy number variation1nstd166human GRCh37.p13 chr12: 113,713,533-113,763,570 , GRCh38.p12 chr12: 113,275,728-113,325,765 , TPCN1, 2 more genes
    nsv3914285copy number variation1nstd102humanPathogenic GRCh38 chr12: 113,077,775-114,372,366 , NCBI36 chr12: 111,999,963-113,294,554 , GRCh37 chr12: 113,515,580-114,810,171 RITA1, DTX1, 27 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
    nsv3156916copy number variation1nstd151human GRCh37 chr12: 113,495,995-113,909,308 , GRCh38.p12 chr12: 113,058,190-113,471,503 , SDS, 15 more genes
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