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Items: 1 to 20 of 35

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv471696copy number variation12nstd32human NCBI34 chr17: 13,675,157-13,854,135 , GRCh37.p13 chr17: 13,474,591-13,653,569 , GRCh38.p12 chr17: 13,571,274-13,750,252 HS3ST3A1, LOC105371544
    nsv471658copy number variation79nstd32human GRCh38.p12 chr21: 9,886,669-10,112,700 , NCBI34 chr9: 43,184,378-43,416,941 , GRCh37.p13 chr9: 45,448,738-46,055,884 LOC105372733, LOC105372734, 1 more genes
    nsv471599copy number variation36nstd32human NCBI34 chrX: 423,855-595,665 , GRCh37.p13 chrX: 481,676-653,486 , GRCh38.p12 chrX: 520,941-692,751 SHOX, KRT18P53, 1 more genes
    nsv471677copy number variation43nstd32human NCBI34 chr1: 103,532,648-103,647,985 , GRCh38.p12 chr1: 103,635,373-103,750,710 , GRCh37.p13 chr1: 104,177,995-104,293,332 AMY1A, AMY1B, 3 more genes
    nsv471691copy number variation19nstd32human NCBI34 chr16: 22,446,888-22,652,575 , GRCh38.p12 chr16: 22,469,014-22,674,701 , GRCh37.p13 chr16: 22,480,335-22,686,022 SMG1P1, OTOAP1, 3 more genes
    nsv471701copy number variation15nstd32human GRCh37.p13 chr17: 45,511,583-45,698,942 , NCBI34 chr17: 45,986,221-46,173,580 , GRCh38.p12 chr17: 47,434,217-47,621,576 NPEPPS, EFCAB13, 2 more genes
    nsv471606copy number variation28nstd32human NCBI34 chrX: 139,339,685-139,508,211 , GRCh37.p13 chrX: 140,646,083-140,814,609 , GRCh38.p12 chrX: 141,558,014-141,726,425 , GRCh37.p13 chrX|NW_004070888.1: 653,817-822,228 SPANXA1, SPANXD, 3 more genes
    nsv471692copy number variation24nstd32human NCBI34 chr16: 32,585,216-32,745,821 , GRCh38.p12 chr16: 32,537,598-32,698,203 , GRCh37.p13 chr16: 32,548,919-32,709,524 TP53TG3, FAM153DP, 2 more genes
    nsv471705copy number variation24nstd32human GRCh38.p12 chr19: 8,650,622-8,802,639 , GRCh37.p13 chr19: 8,760,094-8,875,733 , NCBI34 chr19: 8,621,094-8,774,315 , GRCh37.p13 chr19|NW_003871094.1: 80,592-195,027 ACTL9, OR2Z1, 2 more genes
    nsv471698copy number variation76nstd32human GRCh37.p13 chr17: 44,079,479-44,378,253 , NCBI34 chr17: 44,554,955-44,853,669 , GRCh38.p12 chr17: 46,002,113-46,300,887 MAPT, LRRC37A, 7 more genes
    nsv471661copy number variation135nstd32human NCBI34 chr9: 64,805,733-65,060,890 , GRCh38.p12 chr9: 63,542,269-63,776,777 , GRCh37.p13 chr9: 68,138,003-68,372,511 CDK2AP2P3, RPL7AP46, 5 more genes
    nsv471622copy number variation26nstd32human NCBI34 chr1: 11,924,810-12,112,733 , GRCh38.p12 chr1: 12,155,207-12,371,588 , GRCh37.p13 chr1: 12,215,264-12,431,643 TNFRSF1B, VPS13D, 4 more genes
    nsv471595copy number variation34nstd32human NCBI34 chr22: 19,757,626-19,940,794 , GRCh38.p12 chr22: 21,078,783-21,261,951 , GRCh37.p13 chr22: 21,433,072-21,616,240 E2F6P2, BCRP2, 6 more genes
    nsv471709copy number variation15nstd32human NCBI34 chr22: 14,459,180-14,636,895 , GRCh38.p12 chr22: 15,721,068-15,898,783 , GRCh37.p13 chr22: 16,093,477-16,256,895 POTEH, DUXAP8, 7 more genes
    nsv471678copy number variation26nstd32human NCBI34 chr15: 26,528,591-26,692,594 , GRCh38.p12 chr15: 28,555,640-28,719,643 , GRCh37.p13 chr15: 28,800,786-28,964,789 , GRCh38.p12 chr15|NW_011332701.1: 717,645-881,647 , GRCh38.p12 chr15|NT_187660.1: 831,431-995,433 HERC2P9, GOLGA8M, 6 more genes
    nsv471708copy number variation18nstd32human GRCh38.p12 chr21: 13,537,696-13,701,010 , NCBI34 chr21: 13,831,888-13,995,202 , GRCh37.p13 chr21: 14,910,017-15,073,331 OR4K12P, OR4K11P, 6 more genes
    nsv471625copy number variation25nstd32human GRCh38.p12 chr4: 69,250,956-69,410,069 , GRCh37.p13 chr4: 70,116,674-70,275,787 , NCBI34 chr4: 70,432,219-70,591,332 UGT2B28, UGT2B25P, 6 more genes
    nsv471643copy number variation29nstd32human NCBI34 chr7: 101,763,595-101,920,490 , GRCh37.p13 chr7: 102,203,036-102,359,973 , GRCh38.p12 chr7: 102,562,589-102,719,526 RASA4, POLR2J2, 5 more genes
    nsv471695copy number variation17nstd32human NCBI34 chr16: 69,881,697-70,033,105 , GRCh38.p12 chr16: 70,071,589-70,222,996 , GRCh37.p13 chr16: 70,105,492-70,256,899 PDPR, CLEC18C, 4 more genes
    nsv471594copy number variation65nstd32human NCBI34 chr22: 16,933,332-17,244,196 , GRCh38.p12 chr22: 18,076,012-18,882,129 , GRCh37.p13 chr22: 18,558,778-18,869,642 GGT3P, USP18, 29 more genes
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