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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5492004copy number variation1nstd206human GRCh38 chr10: 100,517,442-100,523,134 , GRCh37.p13 chr10: 102,277,199-102,282,891 NDUFB8, SEC31B
    nsv5489745copy number variation1nstd206human GRCh38 chr10: 100,454,549-100,509,731 , GRCh37.p13 chr10: 102,214,306-102,269,488 , SEC31B, 1 more genes
    nsv5186795mobile element insertion1nstd203human GRCh38 chr10: 100,503,772-100,503,772 , GRCh37.p13 chr10: 102,263,529-102,263,529 SEC31B
    nsv4970294copy number variation1nstd200human GRCh38 chr10: 100,510,378-100,514,448 , GRCh37.p13 chr10: 102,270,135-102,274,205 SEC31B
    nsv4836364copy number variation1nstd200human GRCh37 chr10: 102,214,306-102,269,488 , GRCh38.p12 chr10: 100,454,549-100,509,731 , WNT8B, 1 more genes
    nsv4674975copy number variation1nstd102humanUncertain significance GRCh37 chr10: 101,932,457-102,392,841 , GRCh38.p12 chr10: 100,172,700-100,633,084 NDUFB8, SNORA12, 12 more genes
    nsv4427025copy number variation1nstd174human GRCh37 chr10: 102,213,492-102,269,947 , GRCh38.p12 chr10: 100,453,735-100,510,190 , SEC31B, 1 more genes
    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
    nsv4186973copy number variation1nstd166human GRCh37.p13 chr10: 102,265,655-102,265,874 , GRCh38.p12 chr10: 100,505,898-100,506,117 SEC31B
    nsv4183317copy number variation1nstd166human GRCh37.p13 chr10: 102,268,261-102,275,944 , GRCh38.p12 chr10: 100,508,504-100,516,187 SEC31B
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 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
    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
    nsv3902271copy number variation2nstd102humanPathogenic GRCh37 chr10: 100,027-135,427,143 , GRCh38.p12 chr10: 54,087-133,613,639 ANXA11, EDRF1-DT, 2085 more genes
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