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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv6937823copy number variation1nstd229human GRCh38 chr12: 101,362,526-101,363,181 , GRCh37.p13 chr12: 101,756,304-101,756,959 UTP20
    nsv6936782copy number variation1nstd229human GRCh38 chr12: 101,281,901-101,297,500 , GRCh37.p13 chr12: 101,675,679-101,691,278 UTP20
    nsv6933029copy number variation1nstd229human GRCh38 chr12: 100,269,016-101,400,896 , GRCh37.p13 chr12: 100,662,794-101,794,674 PIGAP1, SCYL2, 10 more genes
    nsv6925532copy number variation1nstd229human GRCh38 chr12: 101,317,401-101,324,600 , GRCh37.p13 chr12: 101,711,179-101,718,378 UTP20
    nsv6923055copy number variation1nstd229human GRCh38 chr12: 101,269,408-101,279,341 , GRCh37.p13 chr12: 101,663,186-101,673,119 UTP20
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
    nsv6920808copy number variation1nstd229human GRCh38 chr12: 101,366,901-101,498,500 , GRCh37.p13 chr12: 101,760,679-101,892,278 UTP20, RNA5SP367, 5 more genes
    nsv6919034copy number variation1nstd229human GRCh38 chr12: 101,376,921-101,392,596 , GRCh37.p13 chr12: 101,770,699-101,786,374 ARL1, UTP20
    nsv6637713copy number variation1nstd102humanUncertain significance GRCh37 chr12: 101,272,963-101,745,632 , GRCh38.p12 chr12: 100,879,185-101,351,854 RPS6P19, UTP20, 4 more genes
    nsv6621394copy number variation1nstd224human GRCh37 chr12: 101,381,343-102,057,252 , GRCh38.p12 chr12: 100,987,565-101,663,474 ANO4, RNU5E-5P, 14 more genes
    nsv6586131inversion1nstd223human GRCh38 chr12: 101,341,076-101,341,661 , GRCh37.p13 chr12: 101,734,854-101,735,439 UTP20
    nsv6585570inversion1nstd223human GRCh38 chr12: 101,301,380-101,301,956 , GRCh37.p13 chr12: 101,695,158-101,695,734 UTP20
    nsv6577147inversion1nstd223human GRCh38 chr12: 101,347,412-101,347,839 , GRCh37.p13 chr12: 101,741,190-101,741,617 UTP20
    nsv6474842copy number variation1nstd223human GRCh38 chr12: 101,362,526-101,363,179 , GRCh37.p13 chr12: 101,756,304-101,756,957 UTP20
    nsv6464038copy number variation1nstd223human GRCh38 chr12: 101,269,404-101,279,340 , GRCh37.p13 chr12: 101,663,182-101,673,118 UTP20
    nsv6313913copy number variation1nstd102humanUncertain significance GRCh37 chr12: 100,564,593-103,021,075 , GRCh38.p12 chr12: 100,170,815-102,627,297 DEPDC4, SLC5A8, 46 more genes
    nsv6288966insertion1nstd214human GRCh38 chr12: 101,362,526-101,362,526 , GRCh37.p13 chr12: 101,756,304-101,756,304 UTP20
    nsv6191079copy number variation1nstd214human GRCh38 chr12: 101,328,245-101,328,305 , GRCh37.p13 chr12: 101,722,023-101,722,083 UTP20
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