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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3873027copy number variation1nstd102humanBenign GRCh37 chr3: 139,641,010-139,667,945 , GRCh38.p12 chr3: 139,922,168-139,949,103 CLSTN2
    nsv3883960copy number variation1nstd102humanBenign GRCh37 chr3: 139,632,361-139,654,211 , GRCh38.p12 chr3: 139,913,519-139,935,369 CLSTN2
    nsv3873594copy number variation1nstd102humanBenign GRCh37 chr3: 139,635,017-139,654,211 , GRCh38.p12 chr3: 139,916,175-139,935,369 CLSTN2
    nsv3885726copy number variation1nstd102humanBenign GRCh37 chr3: 139,636,462-139,654,211 , GRCh38.p12 chr3: 139,917,620-139,935,369 CLSTN2
    nsv3879816copy number variation1nstd102humanBenign GRCh37 chr3: 139,641,010-139,654,211 , GRCh38.p12 chr3: 139,922,168-139,935,369 CLSTN2
    nsv3876488copy number variation1nstd102humanBenign GRCh37 chr3: 139,648,874-139,654,187 , GRCh38.p12 chr3: 139,930,032-139,935,345 CLSTN2
    nsv3878094copy number variation1nstd102humanBenign GRCh37 chr3: 139,653,776-139,654,211 , GRCh38.p12 chr3: 139,934,934-139,935,369 CLSTN2
    nsv3872954copy number variation1nstd102humanBenign GRCh37 chr3: 139,653,811-139,654,211 , GRCh38.p12 chr3: 139,934,969-139,935,369 CLSTN2
    nsv3871370copy number variation1nstd102humanBenign GRCh37 chr3: 139,653,811-139,654,187 , GRCh38.p12 chr3: 139,934,969-139,935,345 CLSTN2
    nsv3883376copy number variation1nstd102humanBenign GRCh37 chr3: 139,979,100-140,169,657 , GRCh38.p12 chr3: 140,260,258-140,450,815 CLSTN2, LOC105374132
    nsv3880426copy number variation1nstd102humanBenign GRCh37 chr3: 139,409,436-139,922,915 , GRCh38.p12 chr3: 139,690,594-140,204,073 CLSTN2, TRMT112P5
    nsv3887843copy number variation1nstd102humanLikely benign GRCh37 chr3: 139,518,439-139,944,213 , GRCh38.p12 chr3: 139,799,597-140,225,371 CLSTN2, TRMT112P5
    nsv3887611copy number variation1nstd102humanBenign GRCh37 chr3: 140,014,763-140,180,563 , GRCh38.p12 chr3: 140,295,921-140,461,721 CLSTN2, LOC105374132
    nsv6291050copy number variation1nstd102humanUncertain significance GRCh37 chr3: 139,339,589-139,659,995 , GRCh38.p12 chr3: 139,620,747-139,941,153 CLSTN2, TRMT112P5, 1 more genes
    nsv3920790copy number variation1nstd102humanPathogenic GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325 CLSTN2, TFDP2, 203 more genes
    nsv3920279copy number variation1nstd102humanPathogenic GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156 CLSTN2, NPHP3-AS1, 218 more genes
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 CLSTN2, BFSP2, 169 more genes
    nsv3914757copy number variation1nstd102humanPathogenic NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997 CLSTN2, CLSTN2-AS1, 177 more genes
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 CLSTN2, A4GNT, 134 more genes
    nsv3910942copy number variation1nstd102humanPathogenic NCBI36 chr3: 135,535,085-142,902,990 , GRCh38 chr3: 134,333,553-141,701,458 , GRCh37 chr3: 134,052,395-141,420,300 CLSTN2, MRAS, 96 more genes
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