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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146775insertion1nstd232human GRCh37.p13 chr12: 103,994,631-103,994,631 , GRCh38.p12 chr12: 103,600,853-103,600,853 STAB2
    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
    nsv6936454copy number variation1nstd229human GRCh38 chr12: 103,649,935-103,708,060 , GRCh37.p13 chr12: 104,043,713-104,101,838 STAB2, LOC105369946
    nsv6935154copy number variation1nstd229human GRCh38 chr12: 103,726,643-103,726,874 , GRCh37.p13 chr12: 104,120,421-104,120,652 STAB2
    nsv6934941copy number variation1nstd229human GRCh38 chr12: 103,742,288-103,745,825 , GRCh37.p13 chr12: 104,136,066-104,139,603 STAB2, NT5DC3
    nsv6931708copy number variation1nstd229human GRCh38 chr12: 103,703,731-103,820,607 , GRCh37.p13 chr12: 104,097,509-104,214,385 STAB2, NT5DC3
    nsv6931477copy number variation1nstd229human GRCh38 chr12: 103,630,228-103,641,914 , GRCh37.p13 chr12: 104,024,006-104,035,692 STAB2
    nsv6930442copy number variation1nstd229human GRCh38 chr12: 103,650,401-103,666,000 , GRCh37.p13 chr12: 104,044,179-104,059,778 STAB2, LOC105369946
    nsv6930085copy number variation1nstd229human GRCh38 chr12: 103,672,416-103,678,804 , GRCh37.p13 chr12: 104,066,194-104,072,582 LOC105369946, STAB2
    nsv6930052copy number variation1nstd229human GRCh38 chr12: 103,650,412-103,666,020 , GRCh37.p13 chr12: 104,044,190-104,059,798 LOC105369946, STAB2
    nsv6927851copy number variation1nstd229human GRCh38 chr12: 103,631,326-103,632,776 , GRCh37.p13 chr12: 104,025,104-104,026,554 STAB2
    nsv6927843copy number variation1nstd229human GRCh38 chr12: 103,686,297-103,702,710 , GRCh37.p13 chr12: 104,080,075-104,096,488 STAB2
    nsv6927288copy number variation1nstd229human GRCh38 chr12: 103,679,123-103,681,658 , GRCh37.p13 chr12: 104,072,901-104,075,436 STAB2
    nsv6926789copy number variation1nstd229human GRCh38 chr12: 103,738,546-103,743,260 , GRCh37.p13 chr12: 104,132,324-104,137,038 STAB2
    nsv6925756copy number variation1nstd229human GRCh38 chr12: 103,582,022-103,587,173 , GRCh37.p13 chr12: 103,975,800-103,980,951 STAB2
    nsv6925749copy number variation1nstd229human GRCh38 chr12: 103,607,301-103,613,900 , GRCh37.p13 chr12: 104,001,079-104,007,678 STAB2
    nsv6924371copy number variation1nstd229human GRCh38 chr12: 103,720,752-103,724,750 , GRCh37.p13 chr12: 104,114,530-104,118,528 STAB2
    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
    nsv6922288copy number variation1nstd229human GRCh38 chr12: 103,719,141-103,719,452 , GRCh37.p13 chr12: 104,112,919-104,113,230 STAB2
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