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Items: 1 to 20 of 255

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944834copy number variation1nstd209human GRCh38 chr13: 99,531,113-99,533,920 , GRCh37.p13 chr13: 100,183,367-100,186,174 TM9SF2
    nsv5861334copy number variation1nstd209human GRCh38 chr13: 99,531,098-99,533,714 , GRCh37.p13 chr13: 100,183,352-100,185,968 TM9SF2
    nsv5728075mobile element insertion1nstd211human GRCh38 chr13: 99,517,120-99,517,120 , GRCh37.p13 chr13: 100,169,374-100,169,374 TM9SF2
    nsv5719686mobile element insertion1nstd211human GRCh38 chr13: 99,542,566-99,542,566 , GRCh37.p13 chr13: 100,194,820-100,194,820 TM9SF2
    nsv5710211mobile element insertion1nstd211human GRCh38 chr13: 99,511,844-99,511,844 , GRCh37.p13 chr13: 100,164,098-100,164,098 TM9SF2
    nsv5706048mobile element insertion1nstd211human GRCh38 chr13: 99,517,877-99,517,877 , GRCh37.p13 chr13: 100,170,131-100,170,131 TM9SF2
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5562852mobile element insertion1nstd206human GRCh38 chr13: 99,542,566-99,542,617 , GRCh37.p13 chr13: 100,194,820-100,194,871 TM9SF2
    nsv5504977copy number variation1nstd206human GRCh38 chr13: 99,538,682-99,539,024 , GRCh37.p13 chr13: 100,190,936-100,191,278 TM9SF2
    nsv5500931copy number variation1nstd206human GRCh38 chr13: 99,502,175-99,502,244 , GRCh37.p13 chr13: 100,154,429-100,154,498 TM9SF2
    nsv5187507mobile element insertion1nstd203human GRCh38 chr13: 99,517,106-99,517,120 , GRCh37.p13 chr13: 100,169,360-100,169,374 TM9SF2
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4998389copy number variation1nstd200human GRCh38 chr13: 99,564,337-99,565,288 , GRCh37.p13 chr13: 100,216,591-100,217,542 TM9SF2
    nsv4998388copy number variation1nstd200human GRCh38 chr13: 99,504,524-99,515,799 , GRCh37.p13 chr13: 100,156,778-100,168,053 TM9SF2
    nsv4993914copy number variation1nstd200human GRCh38 chr13: 99,538,576-99,539,022 , GRCh37.p13 chr13: 100,190,830-100,191,276 TM9SF2
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4832556copy number variation1nstd200human GRCh37 chr13: 100,207,212-100,207,490 , GRCh38.p12 chr13: 99,554,958-99,555,236 TM9SF2
    nsv4683528copy number variation1nstd102humanPathogenic GRCh37 chr13: 100,038,233-100,638,902 , GRCh38.p12 chr13: 99,385,979-99,986,648 CLYBL-AS2, RNY3P6, 14 more genes
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