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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv6968449copy number variation1nstd229human GRCh38 chr15: 63,293,988-63,297,371 , GRCh37.p13 chr15: 63,586,187-63,589,570 APH1B
    nsv6963579copy number variation1nstd229human GRCh38 chr15: 63,222,593-63,443,339 , GRCh37.p13 chr15: 63,514,792-63,735,538 RAB8B, APH1B, 2 more genes
    nsv6960684copy number variation1nstd229human GRCh38 chr15: 62,287,754-63,705,691 , GRCh37.p13 chr15: 62,579,953-63,997,890 MIR8067, RPS27L, 21 more genes
    nsv6960212copy number variation1nstd229human GRCh38 chr15: 63,245,676-63,441,189 , GRCh37.p13 chr15: 63,537,875-63,733,388 RAB8B, APH1B, 2 more genes
    nsv6638005copy number variation1nstd102humanUncertain significance GRCh37 chr15: 63,560,124-63,637,751 , GRCh38.p12 chr15: 63,267,925-63,345,552 APH1B, RAB8B, 1 more genes
    nsv6588207inversion1nstd223human GRCh38 chr15: 63,303,132-63,304,323 , GRCh37.p13 chr15: 63,595,331-63,596,522 APH1B
    nsv6507846copy number variation1nstd223human GRCh38 chr15: 63,293,988-63,297,367 , GRCh37.p13 chr15: 63,586,187-63,589,566 APH1B
    nsv6249751mobile element insertion1nstd215human GRCh38 chr15: 63,287,366-63,287,366 , GRCh37.p13 chr15: 63,579,565-63,579,565 APH1B
    nsv6249750mobile element insertion1nstd215human GRCh38 chr15: 63,287,086-63,287,086 , GRCh37.p13 chr15: 63,579,285-63,579,285 APH1B
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv6095343insertion1nstd212human GRCh38 chr15: 63,287,352-63,287,352 , GRCh37.p13 chr15: 63,579,551-63,579,551 APH1B
    nsv5704254mobile element insertion2nstd211human GRCh38 chr15: 63,287,366-63,287,366 , GRCh37.p13 chr15: 63,579,565-63,579,565 APH1B
    nsv5516646copy number variation1nstd206human GRCh38 chr15: 63,275,531-63,275,603 , GRCh37.p13 chr15: 63,567,730-63,567,802 APH1B
    nsv5423478mobile element insertion1nstd206human GRCh38 chr15: 63,287,366-63,287,417 , GRCh37.p13 chr15: 63,579,565-63,579,616 APH1B
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5140536mobile element insertion1nstd203human GRCh38 chr15: 63,287,584-63,287,600 , GRCh37.p13 chr15: 63,579,783-63,579,799 APH1B
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
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