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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074287inversion1nstd229human GRCh38 chr12: 91,708,373-92,319,944 , GRCh37.p13 chr12: 92,102,150-92,713,720 LINC01619, LINC02391, 5 more genes
    nsv7072173inversion1nstd229human GRCh38 chr12: 92,142,471-92,142,487 , GRCh37.p13 chr12: 92,536,247-92,536,263 BTG1, LINC01619
    nsv7062138inversion1nstd229human GRCh38 chr12: 91,752,522-94,050,052 , GRCh37.p13 chr12: 92,146,299-94,443,828 , NUDT4, 40 more genes
    nsv6932636copy number variation1nstd229human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 BTG1, LINC01619
    nsv6930968copy number variation1nstd229human GRCh38 chr12: 92,083,487-92,140,124 , GRCh37.p13 chr12: 92,477,263-92,533,900 LINC01619, BTG1
    nsv6928740copy number variation1nstd229human GRCh38 chr12: 92,144,101-92,164,000 , GRCh37.p13 chr12: 92,537,877-92,557,776 BTG1, BTG1-DT
    nsv6460751copy number variation1nstd223human GRCh38 chr12: 92,116,508-92,143,100 , GRCh37.p13 chr12: 92,510,284-92,536,876 BTG1, LINC01619
    nsv6455871copy number variation1nstd223human GRCh38 chr12: 92,144,701-92,146,600 , GRCh37.p13 chr12: 92,538,477-92,540,376 BTG1-DT, BTG1
    nsv6313949copy number variation1nstd102humanUncertain significance GRCh37 chr12: 91,073,628-92,829,926 , GRCh38.p12 chr12: 90,679,851-92,436,150 LOC105369896, LINC00615, 20 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132715copy number variation1nstd213human GRCh37 chr12: 84,440,000-93,800,001 , GRCh38.p12 chr12: 84,046,221-93,406,225 , BTG1, 102 more genes
    nsv6132519copy number variation1nstd213human GRCh37 chr12: 91,620,000-94,700,001 , GRCh38.p12 chr12: 91,226,223-94,306,225 , BTG1, 46 more genes
    nsv6132448copy number variation1nstd213human GRCh37 chr12: 91,550,000-94,690,001 , GRCh38.p12 chr12: 91,156,223-94,296,225 , BTG1, 47 more genes
    nsv5509709copy number variation1nstd206human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 LINC01619, BTG1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4993553copy number variation1nstd200human GRCh38 chr12: 92,116,508-92,143,103 , GRCh37.p13 chr12: 92,510,284-92,536,879 BTG1, LINC01619
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4843573copy number variation1nstd200human GRCh37 chr12: 92,510,284-92,536,879 , GRCh38.p12 chr12: 92,116,508-92,143,103 LINC01619, BTG1
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