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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5704815mobile element insertion2nstd211human GRCh38 chr10: 99,749,548-99,749,548 , GRCh37.p13 chr10: 101,509,305-101,509,305 CUTC
    nsv5638648insertion1nstd207human GRCh38 chr10: 99,749,532-99,749,532 , GRCh37.p13 chr10: 101,509,289-101,509,289 CUTC
    nsv5542177insertion1nstd206human GRCh38 chr10: 99,749,548-99,749,599 , GRCh37.p13 chr10: 101,509,305-101,509,356 CUTC
    nsv5493706copy number variation1nstd206human GRCh38 chr10: 99,728,233-99,730,847 , GRCh37.p13 chr10: 101,487,990-101,490,604 COX15, CUTC
    nsv5138652mobile element insertion1nstd203human GRCh38 chr10: 99,749,532-99,749,548 , GRCh37.p13 chr10: 101,509,289-101,509,305 CUTC
    nsv4495889mobile element insertion1nstd166human GRCh37.p13 chr10: 101,509,289-101,509,289 , GRCh38.p12 chr10: 99,749,532-99,749,532 CUTC
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv4178927copy number variation1nstd166human GRCh37.p13 chr10: 101,505,469-101,515,107 , GRCh38.p12 chr10: 99,745,712-99,755,350 CUTC
    nsv4178880copy number variation1nstd166human GRCh37.p13 chr10: 101,471,297-101,783,479 , GRCh38.p12 chr10: 99,711,540-100,023,722 ABCC2, COX15, 5 more genes
    nsv3968219insertion1nstd168human GRCh38 chr10: 99,749,226-99,753,349 , GRCh37.p13 chr10: 101,508,983-101,513,106 CUTC
    nsv3921251copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,093,697-102,235,324 , NCBI36 chr10: 101,083,687-102,225,314 , GRCh38 chr10: 99,333,940-100,475,567 CUTC, COX15, 29 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3911966copy number variation1nstd102humanUncertain significance NCBI36 chr10: 101,466,071-101,749,704 , GRCh38 chr10: 99,716,324-99,999,957 , GRCh37 chr10: 101,476,081-101,759,714 NANOGP6, CUTC, 4 more genes
    nsv3911437copy number variation1nstd102humanPathogenic GRCh38 chr10: 93,181,201-101,356,779 , NCBI36 chr10: 94,930,948-103,106,526 , GRCh37 chr10: 94,940,958-103,116,536 SLF2, CUTC, 171 more genes
    nsv3911005copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,146,389-102,407,978 , NCBI36 chr10: 101,136,379-102,397,968 , GRCh38 chr10: 99,386,632-100,648,221 NDUFB8, MTATP8P4, 32 more genes
    nsv3909942copy number variation1nstd102humanPathogenic GRCh37 chr10: 96,872,364-118,383,651 , GRCh38 chr10: 95,112,607-116,776,637 , NCBI36 chr10: 96,862,354-118,526,138 LOC102723665, SFR1, 360 more genes
    nsv3907664copy number variation1nstd102humandrug response GRCh37 chr10: 42,347,406-135,534,747 , GRCh38.p12 chr10: 42,101,241-133,787,422 SHOC2, FAM245B, 1487 more genes
    nsv3906389copy number variation1nstd102humanPathogenic GRCh37 chr10: 73,232-135,524,321 , GRCh38.p12 chr10: 27,296-133,786,996 LOC100419870, LOC102724439, 2105 more genes
    nsv3905489copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,283,493-135,427,143 , GRCh38.p12 chr10: 91,523,736-133,613,639 LOC105378476, SMC3, 688 more genes
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