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Items: 1 to 20 of 214

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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
    nsv7062138inversion1nstd229human GRCh38 chr12: 91,752,522-94,050,052 , GRCh37.p13 chr12: 92,146,299-94,443,828 , NUDT4, 40 more genes
    nsv6936605copy number variation1nstd229human GRCh38 chr12: 92,152,112-92,157,007 , GRCh37.p13 chr12: 92,545,888-92,550,783 BTG1-DT
    nsv6928740copy number variation1nstd229human GRCh38 chr12: 92,144,101-92,164,000 , GRCh37.p13 chr12: 92,537,877-92,557,776 BTG1, BTG1-DT
    nsv6921224copy number variation1nstd229human GRCh38 chr12: 92,149,701-92,153,000 , GRCh37.p13 chr12: 92,543,477-92,546,776 BTG1-DT
    nsv6920713copy number variation1nstd229human GRCh38 chr12: 92,166,130-92,172,961 , GRCh37.p13 chr12: 92,559,906-92,566,737 BTG1-DT, RPL21P106
    nsv6581558inversion1nstd223human GRCh38 chr12: 92,152,777-92,153,226 , GRCh37.p13 chr12: 92,546,553-92,547,002 BTG1-DT
    nsv6579522inversion1nstd223human GRCh38 chr12: 92,160,402-92,161,379 , GRCh37.p13 chr12: 92,554,178-92,555,155 BTG1-DT
    nsv6475399copy number variation1nstd223human GRCh38 chr12: 92,169,001-92,169,800 , GRCh37.p13 chr12: 92,562,777-92,563,576 RPL21P106, BTG1-DT
    nsv6474600copy number variation1nstd223human GRCh38 chr12: 92,170,430-92,171,298 , GRCh37.p13 chr12: 92,564,206-92,565,074 BTG1-DT
    nsv6461143copy number variation1nstd223human GRCh38 chr12: 92,165,214-92,165,812 , GRCh37.p13 chr12: 92,558,990-92,559,588 BTG1-DT
    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
    nsv6037532copy number variation1nstd212human GRCh38 chr12: 92,153,347-92,153,451 , GRCh37.p13 chr12: 92,547,123-92,547,227 , BTG1-DT
    nsv5700945mobile element insertion1nstd211human GRCh38 chr12: 92,167,525-92,167,525 , GRCh37.p13 chr12: 92,561,301-92,561,301 RPL21P106, BTG1-DT
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
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