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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061866inversion1nstd229human GRCh38 chr8: 57,193,747-57,298,077 , GRCh37.p13 chr8: 58,106,306-58,210,636 LINC00588, LOC286177, 2 more genes
    nsv6846978copy number variation1nstd229human GRCh38 chr8: 57,231,610-57,293,001 , GRCh37.p13 chr8: 58,144,169-58,205,560 LINC00588, LINC01606, 2 more genes
    nsv6841828copy number variation1nstd229human GRCh38 chr8: 57,222,355-57,308,184 , GRCh37.p13 chr8: 58,134,914-58,220,743 LOC286177, LINC01606, 2 more genes
    nsv6569954inversion1nstd223human GRCh38 chr8: 50,962,824-58,188,676 , GRCh37.p13 chr8: 51,875,384-59,101,235 LOC101929398, LOC107986888, 98 more genes
    nsv6431324copy number variation1nstd223human GRCh38 chr8: 57,283,166-57,283,523 , GRCh37.p13 chr8: 58,195,725-58,196,082 LINC00588
    nsv6423861copy number variation1nstd223human GRCh38 chr8: 57,261,784-57,280,842 , GRCh37.p13 chr8: 58,174,343-58,193,401 LOC286177, LINC00588
    nsv6420232copy number variation1nstd223human GRCh38 chr8: 57,222,355-57,308,184 , GRCh37.p13 chr8: 58,134,914-58,220,743 LINC01606, RNU6-596P, 2 more genes
    nsv6136681copy number variation1nstd213human GRCh37 chr8: 46,860,000-86,550,001 , GRCh38.p12 chr8: 45,948,378-85,637,772 CEBPD, EYA1, 519 more genes
    nsv6136065copy number variation1nstd213human GRCh37 chr8: 56,820,000-59,400,001 , GRCh38.p12 chr8: 55,907,441-58,487,442 LYN, MOS, 42 more genes
    nsv6136061copy number variation1nstd213human GRCh37 chr8: 54,780,000-63,060,001 , GRCh38.p12 chr8: 53,867,440-62,147,442 RAB2A, SDCBP, 117 more genes
    nsv4960407copy number variation1nstd200human GRCh38 chr8: 57,261,779-57,280,871 , GRCh37.p13 chr8: 58,174,338-58,193,430 LOC286177, LINC00588
    nsv4612778copy number variation1nstd183human GRCh37 chr8: 58,053,729-58,201,846 , GRCh38.p12 chr8|NT_187566.1: 48,905-127,701 , GRCh38.p12 chr8: 57,141,170-57,289,287 LINC01606, RNU6-596P, 2 more genes
    nsv4526380copy number variation1nstd166human GRCh37.p13 chr8: 58,194,233-58,200,283 , GRCh38.p12 chr8: 57,281,674-57,287,724 , GRCh38.p12 chr8|NT_187566.1: 120,088-126,138 RNU6-596P, LINC00588
    nsv4525626copy number variation1nstd166human GRCh37.p13 chr8: 58,197,525-58,197,619 , GRCh38.p12 chr8: 57,284,966-57,285,060 , GRCh38.p12 chr8|NT_187566.1: 123,380-123,474 LINC00588
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455349copy number variation1nstd102humanUncertain significance GRCh37 chr8: 57,699,846-58,315,215 , GRCh38.p12 chr8: 56,787,287-57,402,656 LINC00588, LOC286177, 7 more genes
    nsv4404543copy number variation1nstd174human GRCh37 chr8: 58,046,936-58,203,260 , GRCh38.p12 chr8: 57,134,377-57,290,701 , GRCh38.p12 chr8|NT_187566.1: 48,905-129,115 LINC01606, RNU6-596P, 2 more genes
    nsv4369947copy number variation1nstd173human GRCh37 chr8: 58,096,526-58,355,572 , GRCh38.p12 chr8: 57,183,967-57,443,013 LINC00588, LOC286177, 5 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 LOC101929488, TEX15, 2105 more genes
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