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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
    nsv7070589inversion1nstd229human GRCh38 chr18: 72,525,979-73,914,311 , GRCh37.p13 chr18: 70,193,214-71,581,546 RNA5SP460, MIR548AV, 9 more genes
    nsv7015344copy number variation1nstd229human GRCh38 chr18: 72,583,200-72,596,923 , GRCh37.p13 chr18: 70,250,435-70,264,158 CBLN2
    nsv7013540copy number variation1nstd229human GRCh38 chr18: 71,983,964-72,697,931 , GRCh37.p13 chr18: 69,651,200-70,365,166 LOC105372189, HNRNPA1P11, 1 more genes
    nsv7013484copy number variation1nstd229human GRCh38 chr18: 72,607,311-72,617,668 , GRCh37.p13 chr18: 70,274,546-70,284,903 CBLN2, HNRNPA1P11
    nsv7011632copy number variation1nstd229human GRCh38 chr18: 72,545,675-72,600,250 , GRCh37.p13 chr18: 70,212,910-70,267,485 CBLN2
    nsv7010994copy number variation1nstd229human GRCh38 chr18: 72,524,541-72,532,614 , GRCh37.p13 chr18: 70,191,776-70,199,849 CBLN2
    nsv7009023copy number variation1nstd229human GRCh38 chr18: 72,551,979-72,573,522 , GRCh37.p13 chr18: 70,219,214-70,240,757 CBLN2
    nsv7008196copy number variation1nstd229human GRCh38 chr18: 72,635,151-72,635,209 , GRCh37.p13 chr18: 70,302,386-70,302,444 CBLN2
    nsv7007900copy number variation1nstd229human GRCh38 chr18: 72,617,607-72,665,615 , GRCh37.p13 chr18: 70,284,842-70,332,850 CBLN2, HNRNPA1P11
    nsv7005291copy number variation1nstd229human GRCh38 chr18: 72,596,177-72,596,355 , GRCh37.p13 chr18: 70,263,412-70,263,590 CBLN2
    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
    nsv7004342copy number variation1nstd229human GRCh38 chr18: 72,582,951-72,612,324 , GRCh37.p13 chr18: 70,250,186-70,279,559 CBLN2
    nsv7004044copy number variation1nstd229human GRCh38 chr18: 72,524,001-72,531,900 , GRCh37.p13 chr18: 70,191,236-70,199,135 CBLN2
    nsv7003036copy number variation1nstd229human GRCh38 chr18: 72,549,101-72,555,700 , GRCh37.p13 chr18: 70,216,336-70,222,935 CBLN2
    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
    nsv7001741copy number variation1nstd229human GRCh38 chr18: 72,631,534-72,631,717 , GRCh37.p13 chr18: 70,298,769-70,298,952 CBLN2
    nsv7001352copy number variation1nstd229human GRCh38 chr18: 72,566,406-72,574,994 , GRCh37.p13 chr18: 70,233,641-70,242,229 CBLN2
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