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Items: 1 to 20 of 129

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956027insertion1nstd209human GRCh38 chr10: 102,906,268-102,906,268 , GRCh37.p13 chr10: 104,666,025-104,666,025 LOC107984265
    nsv5698047mobile element insertion1nstd211human GRCh38 chr10: 102,916,066-102,916,066 , GRCh37.p13 chr10: 104,675,823-104,675,823 LOC107984265
    nsv5589112copy number variation1nstd207human GRCh38 chr10: 102,911,024-102,911,074 , GRCh37.p13 chr10: 104,670,781-104,670,831 LOC107984265
    nsv5551272insertion1nstd206human GRCh38 chr10: 102,915,225-102,915,260 , GRCh37.p13 chr10: 104,674,982-104,675,017 LOC107984265
    nsv5200334copy number variation1nstd102humanPathogenic GRCh37 chr10: 104,678,237-104,816,721 , GRCh38.p12 chr10: 102,918,480-103,056,964 CNNM2, LOC107984265
    nsv5133205mobile element insertion1nstd203human GRCh38 chr10: 102,915,209-102,915,221 , GRCh37.p13 chr10: 104,674,966-104,674,978 LOC107984265
    nsv4973999copy number variation1nstd200human GRCh38 chr10: 102,917,656-102,919,327 , GRCh37.p13 chr10: 104,677,413-104,679,084 CNNM2, LOC107984265
    nsv4973998copy number variation1nstd200human GRCh38 chr10: 102,897,234-102,906,316 , GRCh37.p13 chr10: 104,656,991-104,666,073 LOC107984265, BORCS7-ASMT, 1 more genes
    nsv4841346copy number variation1nstd200human GRCh37 chr10: 104,656,991-104,666,073 , GRCh38.p12 chr10: 102,897,234-102,906,316 LOC107984265, BORCS7-ASMT, 1 more genes
    nsv4829941copy number variation1nstd200human GRCh37 chr10: 104,672,805-104,676,675 , GRCh38.p12 chr10: 102,913,048-102,916,918 LOC107984265, CNNM2
    nsv4745028copy number variation1nstd199human GRCh37 chr10: 104,670,727-104,670,809 , GRCh38.p12 chr10: 102,910,970-102,911,052 LOC107984265
    nsv4679283copy number variation1nstd189human GRCh37.p13 chr10: 104,468,424-105,156,097 , GRCh38.p12 chr10: 102,708,667-103,396,340 , ARL3, 25 more genes
    nsv4598768copy number variation1nstd183human GRCh37 chr10: 104,661,276-104,661,751 , GRCh38.p12 chr10: 102,901,519-102,901,994 LOC107984265, AS3MT, 1 more genes
    nsv4492689mobile element insertion1nstd166human GRCh37.p13 chr10: 104,674,966-104,674,966 , GRCh38.p12 chr10: 102,915,209-102,915,209 LOC107984265
    nsv4455954copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,651,078-104,718,119 , GRCh38.p12 chr10: 102,891,321-102,958,362 BORCS7-ASMT, AS3MT, 2 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
    nsv4176940copy number variation1nstd166human GRCh37.p13 chr10: 104,675,000-104,681,000 , GRCh38.p12 chr10: 102,915,243-102,921,243 CNNM2, LOC107984265
    nsv3924696copy number variation1nstd102humanPathogenic GRCh38 chr10: 102,243,341-103,929,730 , GRCh37 chr10: 104,003,098-105,689,488 , NCBI36 chr10: 103,993,088-105,679,478 MIR146B, RPL23AP58, 48 more genes
    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
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