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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5312456copy number variation1nstd204human GRCh38.p13 chr10: 103,390,242-103,462,220 , GRCh37.p13 chr10: 105,149,999-105,221,977 ATP5MK, PDCD11, 3 more genes
    nsv5310825copy number variation1nstd204human GRCh37.p13 chr10: 105,208,301-105,213,512 , GRCh38.p13 chr10: 103,448,544-103,453,755 CALHM2, CALHM1
    nsv5249860copy number variation1nstd204human GRCh38.p13 chr10: 103,448,671-103,453,011 , GRCh37.p13 chr10: 105,208,428-105,212,768 CALHM1, CALHM2
    nsv5241420copy number variation1nstd204human GRCh38.p13 chr10: 103,443,996-103,444,995 , GRCh37.p13 chr10: 105,203,753-105,204,752 CALHM2, PDCD11
    nsv4974004copy number variation1nstd200human GRCh38 chr10: 103,392,774-103,551,394 , GRCh37.p13 chr10: 105,152,531-105,311,151 MIR1307, NEURL1-AS1, 6 more genes
    nsv4974003copy number variation1nstd200human GRCh38 chr10: 103,390,468-103,461,970 , GRCh37.p13 chr10: 105,150,225-105,221,727 PDCD11, ATP5MK, 3 more genes
    nsv4970409copy number variation1nstd200human GRCh38 chr10: 103,448,549-103,453,746 , GRCh37.p13 chr10: 105,208,306-105,213,503 CALHM2, CALHM1
    nsv4841933copy number variation1nstd200human GRCh37 chr10: 105,208,306-105,213,503 , GRCh38.p12 chr10: 103,448,549-103,453,746 CALHM2, CALHM1
    nsv4835526copy number variation1nstd200human GRCh37 chr10: 105,150,182-105,221,765 , GRCh38.p12 chr10: 103,390,425-103,462,008 MIR1307, CALHM2, 3 more genes
    nsv4729000copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,883,845-105,482,700 , GRCh38.p12 chr10: 103,124,088-103,722,942 INA, RNU11-3P, 16 more genes
    nsv4675057copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,576-105,241,844 , GRCh38.p12 chr10: 103,155,819-103,482,087 INA, NT5C2, 13 more genes
    nsv4607757copy number variation1nstd183human GRCh37 chr10: 105,151,046-105,216,921 , GRCh38.p12 chr10: 103,391,289-103,457,164 ATP5MK, MIR1307, 3 more genes
    nsv4457357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 104,915,309-105,332,773 , GRCh38.p12 chr10: 103,155,552-103,573,016 PDCD11, TAF5, 14 more genes
    nsv4421330copy number variation1nstd174human GRCh37 chr10: 105,144,930-105,313,230 , GRCh38.p12 chr10: 103,385,173-103,553,473 TAF5, NEURL1, 7 more genes
    nsv4420905copy number variation1nstd174human GRCh37 chr10: 105,144,930-105,224,106 , GRCh38.p12 chr10: 103,385,173-103,464,349 TAF5, PDCD11, 4 more genes
    nsv4386032copy number variation1nstd173human GRCh37 chr10: 105,150,562-105,224,106 , GRCh38.p12 chr10: 103,390,805-103,464,349 CALHM1, PDCD11, 3 more genes
    nsv4373246copy number variation1nstd173human GRCh37 chr10: 105,150,562-105,217,768 , GRCh38.p12 chr10: 103,390,805-103,458,011 CALHM1, MIR1307, 3 more genes
    nsv4368855copy number variation1nstd173human GRCh37 chr10: 105,151,033-105,313,230 , GRCh38.p12 chr10: 103,391,276-103,553,473 CALHM1, NEURL1, 6 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
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