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Items: 1 to 20 of 581

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5973155insertion1nstd209human GRCh38 chr10: 125,919,195-125,919,195 , GRCh37.p13 chr10: 127,607,764-127,607,764 FANK1
    nsv5924914copy number variation1nstd209human GRCh38 chr10: 125,961,505-125,982,297 , GRCh37.p13 chr10: 127,650,074-127,670,866 FANK1-AS1, FANK1
    nsv5921553copy number variation1nstd209human GRCh38 chr10: 125,929,287-125,931,369 , GRCh37.p13 chr10: 127,617,856-127,619,938 FANK1
    nsv5921132copy number variation1nstd209human GRCh38 chr10: 125,982,512-125,983,295 , GRCh37.p13 chr10: 127,671,081-127,671,864 FANK1
    nsv5907738copy number variation1nstd209human GRCh38 chr10: 125,994,112-125,994,171 , GRCh37.p13 chr10: 127,682,681-127,682,740 FANK1
    nsv5857918copy number variation1nstd209human GRCh38 chr10: 125,961,451-125,982,315 , GRCh37.p13 chr10: 127,650,020-127,670,884 FANK1-AS1, FANK1
    nsv5855085copy number variation2nstd209human GRCh38 chr10: 125,977,330-125,980,179 , GRCh37.p13 chr10: 127,665,899-127,668,748 FANK1
    nsv5854507copy number variation1nstd209human GRCh38 chr10: 125,982,191-125,983,390 , GRCh37.p13 chr10: 127,670,760-127,671,959 FANK1
    nsv5850685copy number variation2nstd209human GRCh38 chr10: 125,967,051-125,968,050 , GRCh37.p13 chr10: 127,655,620-127,656,619 FANK1
    nsv5848920copy number variation2nstd209human GRCh38 chr10: 125,980,930-125,982,390 , GRCh37.p13 chr10: 127,669,499-127,670,959 FANK1
    nsv5729513mobile element insertion1nstd211human GRCh38 chr10: 125,897,465-125,897,465 , GRCh37.p13 chr10: 127,586,034-127,586,034 FANK1
    nsv5714734mobile element insertion2nstd211human GRCh38 chr10: 125,925,785-125,925,785 , GRCh37.p13 chr10: 127,614,354-127,614,354 FANK1
    nsv5672526copy number variation1nstd102humanPathogenic GRCh37 chr10: 127,548,166-135,440,251 , GRCh38.p12 chr10: 125,859,597-133,626,747 LINC00601, RPL5P28, 110 more genes
    nsv5633655insertion1nstd207human GRCh38 chr10: 125,925,771-125,925,771 , GRCh37.p13 chr10: 127,614,340-127,614,340 FANK1
    nsv5599166copy number variation1nstd207human GRCh38 chr10: 125,913,273-125,913,351 , GRCh37.p13 chr10: 127,601,842-127,601,920 FANK1
    nsv5560125mobile element insertion1nstd206human GRCh38 chr10: 125,925,785-125,925,836 , GRCh37.p13 chr10: 127,614,354-127,614,405 FANK1
    nsv5553648insertion1nstd206human GRCh38 chr10: 125,914,288-125,914,328 , GRCh37.p13 chr10: 127,602,857-127,602,897 FANK1
    nsv5499203copy number variation1nstd206human GRCh38 chr10: 125,999,079-125,999,154 , GRCh37.p13 chr10: 127,687,648-127,687,723 FANK1
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