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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095423copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,618,104-79,674,270 , GRCh38.p12 chr17: 81,651,074-81,707,240 PDE6G, MRPL12, 5 more genes
    nsv7095371copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,618,104-79,894,690 , GRCh38.p12 chr17: 81,651,074-81,936,814 CCDC137, PPP1R27, 21 more genes
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv6996991copy number variation1nstd229human GRCh38 chr17: 81,663,501-81,669,300 , GRCh37.p13 chr17: 79,630,531-79,636,330 CCDC137, PDE6G, 1 more genes
    nsv6990442copy number variation1nstd229human GRCh38 chr17: 81,605,096-81,723,001 , GRCh37.p13 chr17: 79,572,122-79,690,031 CCDC137, TSPAN10, 8 more genes
    nsv6533054copy number variation1nstd223human GRCh38 chr17: 81,673,784-81,675,488 , GRCh37.p13 chr17: 79,640,814-79,642,518 CCDC137
    nsv6528145copy number variation1nstd223human GRCh38 chr17: 81,673,269-81,678,382 , GRCh37.p13 chr17: 79,640,299-79,645,412 CCDC137
    nsv6527666copy number variation1nstd223human GRCh38 chr17: 81,663,534-81,667,396 , GRCh37.p13 chr17: 79,630,564-79,634,426 PDE6G, CCDC137, 1 more genes
    nsv6526615copy number variation1nstd223human GRCh38 chr17: 81,667,584-81,671,280 , GRCh37.p13 chr17: 79,634,614-79,638,310 CCDC137
    nsv6526209copy number variation1nstd223human GRCh38 chr17: 81,605,096-81,723,001 , GRCh37.p13 chr17: 79,572,122-79,690,031 HGS, SLC25A10, 8 more genes
    nsv6521251copy number variation1nstd223human GRCh38 chr17: 81,669,572-81,669,859 , GRCh37.p13 chr17: 79,636,602-79,636,889 CCDC137
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6133323copy number variation1nstd213human GRCh37 chr17: 78,760,000-81,195,210 , GRCh38.p12 chr17: 80,786,200-83,247,441 , ACTG1, 100 more genes
    nsv6027736copy number variation1nstd212human GRCh38 chr17: 81,663,683-81,664,786 , GRCh37.p13 chr17: 79,630,713-79,631,816 OXLD1, CCDC137
    nsv5938673copy number variation1nstd209human GRCh38 chr17: 81,663,674-81,664,785 , GRCh37.p13 chr17: 79,630,704-79,631,815 CCDC137, OXLD1
    nsv5533474copy number variation1nstd206human GRCh38 chr17: 81,664,652-81,664,771 , GRCh37.p13 chr17: 79,631,682-79,631,801 CCDC137, OXLD1
    nsv5529550copy number variation1nstd206human GRCh38 chr17: 81,663,633-81,664,816 , GRCh37.p13 chr17: 79,630,663-79,631,846 OXLD1, CCDC137
    nsv5349742translocation1nstd200human GRCh38 chr17: 81,674,007-81,674,007 , GRCh38 chr17: 81,674,067-81,674,067 , GRCh37.p13 chr17: 79,641,097-79,641,097 , GRCh37.p13 chr17: 79,641,037-79,641,037 CCDC137
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