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Items: 1 to 20 of 358

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967778inversion1nstd209human GRCh37.p13 chr17: 73,502,206-73,606,416 , GRCh38 chr17: 75,506,125-75,610,335 , LLGL2, 3 more genes
    nsv5932890copy number variation1nstd209human GRCh38 chr17: 75,589,372-75,589,425 , GRCh37.p13 chr17: 73,585,453-73,585,506 MYO15B
    nsv5929357copy number variation1nstd209human GRCh38 chr17: 75,599,454-75,609,030 , GRCh37.p13 chr17: 73,595,535-73,605,111 MYO15B
    nsv5887416copy number variation1nstd209human GRCh38 chr17: 75,585,717-75,598,033 , GRCh37.p13 chr17: 73,581,798-73,594,114 MYO15B
    nsv5882097copy number variation1nstd209human GRCh38 chr17: 75,601,311-75,607,073 , GRCh37.p13 chr17: 73,597,392-73,603,154 MYO15B
    nsv5874990copy number variation1nstd209human GRCh38 chr17: 75,604,224-75,607,509 , GRCh37.p13 chr17: 73,600,305-73,603,590 MYO15B
    nsv5873375copy number variation2nstd209human GRCh38 chr17: 75,598,784-75,601,710 , GRCh37.p13 chr17: 73,594,865-73,597,791 MYO15B
    nsv5589675copy number variation1nstd207human GRCh38 chr17: 75,589,372-75,589,425 , GRCh37.p13 chr17: 73,585,453-73,585,506 MYO15B
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285796copy number variation1nstd204human GRCh37.p13 chr17: 73,542,682-73,669,280 , GRCh38.p13 chr17: 75,546,601-75,673,200 LLGL2, RECQL5, 5 more genes
    nsv5282319copy number variation1nstd204human GRCh38.p13 chr17: 75,609,901-75,917,300 , GRCh37.p13 chr17: 73,605,982-73,913,381 ITGB4, TRIM65, 15 more genes
    nsv5214215mobile element deletion1nstd204human GRCh38.p13 chr17: 75,600,877-75,601,191 , GRCh37.p13 chr17: 73,596,958-73,597,272 MYO15B
    nsv5196477mobile element insertion1nstd203human GRCh38 chr17: 75,585,680-75,585,696 , GRCh37.p13 chr17: 73,581,761-73,581,777 MYO15B
    nsv5149165mobile element insertion1nstd203human GRCh38 chr17: 75,612,524-75,612,529 , GRCh37.p13 chr17: 73,608,605-73,608,610 MYO15B
    nsv5147593mobile element insertion1nstd203human GRCh38 chr17: 75,612,518-75,612,529 , GRCh37.p13 chr17: 73,608,599-73,608,610 MYO15B
    nsv5144521mobile element insertion1nstd203human GRCh38 chr17: 75,612,525-75,612,529 , GRCh37.p13 chr17: 73,608,606-73,608,610 MYO15B
    nsv4907377mobile element deletion1nstd200human GRCh38 chr17: 75,600,886-75,601,183 , GRCh37.p13 chr17: 73,596,967-73,597,264 MYO15B
    nsv4854395copy number variation1nstd200human GRCh37 chr17: 73,595,472-73,605,184 , GRCh38.p12 chr17: 75,599,391-75,609,103 MYO15B
    nsv4854394copy number variation1nstd200human GRCh37 chr17: 73,511,580-73,714,116 , GRCh38.p12 chr17: 75,515,499-75,718,036 , CASKIN2, 8 more genes
    nsv4769563mobile element deletion1nstd200human GRCh37 chr17: 73,596,967-73,597,264 , GRCh38.p12 chr17: 75,600,886-75,601,183 MYO15B
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