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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv6895977copy number variation1nstd229human GRCh38 chr10: 113,439,452-113,787,342 , GRCh37.p13 chr10: 115,199,211-115,547,101 LOC107984270, CASP7, 5 more genes
    nsv6893622copy number variation1nstd229human GRCh38 chr10: 113,574,776-113,587,158 , GRCh37.p13 chr10: 115,334,535-115,346,917 NRAP, HABP2
    nsv6892068copy number variation1nstd229human GRCh38 chr10: 113,495,026-113,757,567 , GRCh37.p13 chr10: 115,254,785-115,517,326 CASP7, NRAP, 2 more genes
    nsv6888476copy number variation1nstd229human GRCh38 chr10: 113,544,134-113,552,780 , GRCh37.p13 chr10: 115,303,893-115,312,539 HABP2
    nsv6887868copy number variation1nstd229human GRCh38 chr10: 113,583,130-113,592,720 , GRCh37.p13 chr10: 115,342,889-115,352,479 NRAP, HABP2
    nsv6886013copy number variation1nstd229human GRCh38 chr10: 113,544,773-113,553,742 , GRCh37.p13 chr10: 115,304,532-115,313,501 HABP2
    nsv6885301copy number variation1nstd229human GRCh38 chr10: 110,780,328-116,002,717 , GRCh37.p13 chr10: 112,540,086-116,786,295 UBE2V1P5, MIR6715A, 66 more genes
    nsv6880389copy number variation1nstd229human GRCh38 chr10: 113,567,186-113,567,245 , GRCh37.p13 chr10: 115,326,945-115,327,004 HABP2
    nsv6620314copy number variation1nstd224human GRCh37 chr10: 115,319,711-115,372,156 , GRCh38.p12 chr10: 113,559,952-113,612,397 HABP2, NRAP
    nsv6620164copy number variation1nstd224human GRCh37 chr10: 115,343,100-115,489,589 , GRCh38.p12 chr10: 113,583,341-113,729,830 HABP2, CASP7, 1 more genes
    nsv6582650inversion1nstd223human GRCh38 chr10: 113,545,861-113,549,407 , GRCh37.p13 chr10: 115,305,620-115,309,166 HABP2
    nsv6454807copy number variation1nstd223human GRCh38 chr10: 113,439,452-113,787,342 , GRCh37.p13 chr10: 115,199,211-115,547,101 CASP7, NRAP, 5 more genes
    nsv6449093copy number variation1nstd223human GRCh38 chr10: 113,562,403-113,563,884 , GRCh37.p13 chr10: 115,322,162-115,323,643 HABP2
    nsv6443022copy number variation1nstd223human GRCh38 chr10: 113,495,026-113,757,564 , GRCh37.p13 chr10: 115,254,785-115,517,323 NRAP, PLEKHS1, 2 more genes
    nsv6314085copy number variation1nstd102humanPathogenic GRCh37 chr10: 108,455,687-135,427,143 , GRCh38.p12 chr10: 106,695,929-133,613,639 LOC107984268, DPYSL4, 379 more genes
    nsv6290874copy number variation1nstd102humanUncertain significance GRCh37 chr10: 107,092,654-117,852,548 , GRCh38.p12 chr10: 105,332,896-116,093,037 MIR6715B, SNRPGP12, 118 more genes
    nsv6132019copy number variation1nstd213human GRCh37 chr10: 115,120,000-116,220,001 , GRCh38.p12 chr10: 113,360,241-114,460,242 CASP7, MIR2110, 21 more genes
    nsv5502465copy number variation1nstd206human GRCh38 chr10: 113,582,352-113,745,283 , GRCh37.p13 chr10: 115,342,111-115,505,042 HABP2, CASP7, 1 more genes
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