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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3891216copy number variation1nstd102humanBenign GRCh37 chr12: 156,857-186,614 , GRCh38.p12 chr12: 47,691-77,448 , GRCh38.p12 chr12|NW_003571049.1: 35,340-71,463 IQSEC3
    nsv3890190copy number variation1nstd102humanBenign/Likely benign GRCh37 chr12: 148,034-176,816 , GRCh38.p12 chr12|NW_003571049.1: 33,495-61,665 , GRCh38.p12 chr12: 45,740-67,650 IQSEC3
    nsv3903348copy number variation1nstd102humanBenign GRCh37 chr12: 292,981-298,500 , GRCh38.p12 chr12: 183,815-189,334 SLC6A12, IQSEC3-AS1
    nsv4684316copy number variation1nstd102humanBenign NCBI36 chr12: 16,001-100,682 , GRCh37 chr12: 70,794-230,421 , GRCh38 chr12|NW_003571049.1: 33,647-115,270 IQSEC3, IQSEC3-AS2
    nsv3910326copy number variation1nstd102humanLikely benign NCBI36 chr12: 100,698-136,086 , GRCh38 chr12: 121,271-156,659 , GRCh37.p13 chr12|NW_003571048.1: 111,271-146,659 IQSEC3, LOC574538
    nsv3906668copy number variation1nstd102humanBenign GRCh37 chr12: 191,619-269,531 , GRCh38.p12 chr12: 82,453-160,365 , GRCh38.p12 chr12|NW_003571049.1: 76,468-154,380 IQSEC3, IQSEC3-AS2, 1 more genes
    nsv3891219copy number variation1nstd102humanBenign GRCh37 chr12: 191,619-263,796 , GRCh38.p12 chr12|NW_003571049.1: 76,468-148,645 , GRCh38.p12 chr12: 82,453-154,630 IQSEC3, IQSEC3-AS2, 1 more genes
    nsv3910307copy number variation1nstd102humanUncertain significance NCBI36 chr12: 18,636-140,673 , GRCh37.p13 chr12: 148,375-270,412 , GRCh38.p12 chr12: 43,334-161,246 , GRCh38.p12 chr12|NW_003571049.1: 33,495-155,261 IQSEC3, LOC574538, 1 more genes
    nsv4455273copy number variation1nstd102humanUncertain significance GRCh37 chr12: 224,051-310,571 , GRCh38.p12 chr12: 114,885-201,405 , GRCh38.p12 chr12|NW_003571049.1: 108,900-167,313 IQSEC3, LOC574538, 2 more genes
    nsv4457052copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926 IQSEC3, TSPAN9, 118 more genes
    nsv3906935copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,201,932 , GRCh38.p12 chr12: 64,620-6,092,766 IQSEC3, LRTM2, 113 more genes
    nsv3907924copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,039,841 , GRCh38.p12 chr12: 64,620-5,930,675 IQSEC3, SLC6A13, 111 more genes
    nsv3901202copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-5,952,112 , GRCh38.p12 chr12: 64,620-5,842,946 IQSEC3, LOC105369595, 110 more genes
    nsv4729176copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329 IQSEC3, RPL18P9, 92 more genes
    nsv3912688copy number variation1nstd102humanPathogenic GRCh37 chr12: 282,465-4,529,751 , NCBI36 chr12: 59,839-4,400,012 , GRCh38 chr12: 80,412-4,420,585 IQSEC3, RPL23AP14, 88 more genes
    nsv3916748copy number variation1nstd102humanPathogenic GRCh37 chr12: 282,465-4,114,078 , NCBI36 chr12: 33,854-3,984,339 , GRCh38 chr12: 54,427-4,004,912 IQSEC3, LAMP1P1, 79 more genes
    nsv3909356copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-4,105,910 , GRCh38.p12 chr12: 64,620-3,996,744 IQSEC3, ITFG2-AS1, 79 more genes
    nsv3910104copy number variation1nstd102humanPathogenic GRCh38 chr12: 121,255-3,968,447 , NCBI36 chr12: 100,682-3,947,874 , GRCh37 chr12: 282,465-4,077,613 IQSEC3, DCP1B, 78 more genes
    nsv3894971copy number variation1nstd102humanPathogenic GRCh37 chr12: 222,888-3,931,052 , GRCh38.p12 chr12: 113,722-3,821,886 IQSEC3, CRACR2A, 75 more genes
    nsv3914833copy number variation1nstd102humanPathogenic GRCh37 chr12: 282,465-3,748,769 , NCBI36 chr12: 33,854-3,619,030 , GRCh38 chr12: 54,427-3,639,603 IQSEC3, NRIP2, 73 more genes
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