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Items: 1 to 20 of 715

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148195copy number variation1nstd102humanPathogenic GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932 LOC105372202, LINC01896, 149 more genes
    nsv7137214copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240 LOC105372228, MIR548AV, 132 more genes
    nsv7099035copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271 LOC107985151, CD226, 129 more genes
    nsv7073685inversion1nstd229human GRCh38 chr18: 72,645,988-74,615,511 , GRCh37.p13 chr18: 70,313,223-72,282,747 LOC105372191, RN7SL551P, 19 more genes
    nsv7070589inversion1nstd229human GRCh38 chr18: 72,525,979-73,914,311 , GRCh37.p13 chr18: 70,193,214-71,581,546 RNA5SP460, MIR548AV, 9 more genes
    nsv7064941inversion1nstd229human GRCh38 chr18: 72,770,666-72,774,500 , GRCh37.p13 chr18: 70,437,901-70,441,735 NETO1
    nsv7017977copy number variation1nstd229human GRCh38 chr18: 72,863,489-72,863,544 , GRCh37.p13 chr18: 70,530,724-70,530,779 NETO1
    nsv7017416copy number variation1nstd229human GRCh38 chr18: 72,820,384-72,825,632 , GRCh37.p13 chr18: 70,487,619-70,492,867 NETO1
    nsv7015693copy number variation1nstd229human GRCh38 chr18: 72,819,001-72,831,900 , GRCh37.p13 chr18: 70,486,236-70,499,135 NETO1
    nsv7011111copy number variation1nstd229human GRCh38 chr18: 72,753,888-72,753,977 , GRCh37.p13 chr18: 70,421,123-70,421,212 NETO1
    nsv7010818copy number variation1nstd229human GRCh38 chr18: 72,808,362-72,823,033 , GRCh37.p13 chr18: 70,475,597-70,490,268 NETO1
    nsv7007769copy number variation1nstd229human GRCh38 chr18: 72,844,710-72,844,749 , GRCh37.p13 chr18: 70,511,945-70,511,984 NETO1
    nsv7006225copy number variation1nstd229human GRCh38 chr18: 72,811,006-72,814,206 , GRCh37.p13 chr18: 70,478,241-70,481,441 NETO1
    nsv7005090copy number variation1nstd229human GRCh38 chr18: 71,829,938-73,504,267 , GRCh37.p13 chr18: 69,497,174-71,171,502 CBLN2, HNRNPA1P11, 8 more genes
    nsv7004756copy number variation1nstd229human GRCh38 chr18: 72,773,542-72,773,634 , GRCh37.p13 chr18: 70,440,777-70,440,869 NETO1
    nsv7004042copy number variation1nstd229human GRCh38 chr18: 72,799,441-72,815,751 , GRCh37.p13 chr18: 70,466,676-70,482,986 NETO1
    nsv7002981copy number variation1nstd229human GRCh38 chr18: 71,069,035-74,330,763 , GRCh37.p13 chr18: 68,736,271-71,997,998 MIR548AV, C18orf63, 24 more genes
    nsv7002531copy number variation1nstd229human GRCh38 chr18: 72,755,709-72,755,773 , GRCh37.p13 chr18: 70,422,944-70,423,008 NETO1
    nsv7001550copy number variation1nstd229human GRCh38 chr18: 72,762,400-72,767,840 , GRCh37.p13 chr18: 70,429,635-70,435,075 NETO1
    nsv6638045copy number variation1nstd102humanPathogenic GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240 LOC105372211, LOC105372188, 128 more genes
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