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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097546copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-80,088,673 , GRCh38.p12 chr5: 80,654,049-80,792,854 MSH3, DHFR
    nsv7097293copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,924,906-80,171,681 , GRCh38.p12 chr5: 80,629,087-80,875,862 DHFR, MTRNR2L2, 2 more genes
    nsv7097161copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-80,040,444 , GRCh38.p12 chr5: 80,654,049-80,744,625 MSH3, DHFR
    nsv7096790copy number variation1nstd102humanPathogenic GRCh37 chr5: 79,949,868-80,074,665 , GRCh38.p12 chr5: 80,654,049-80,778,846 DHFR, MSH3
    nsv7093518insertion1nstd102humanUncertain significance GRCh37 chr5: 79,950,796-79,950,796 , GRCh38 chr5: 80,654,977-80,654,977 DHFR, MSH3
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6776870copy number variation1nstd229human GRCh38 chr5: 80,520,401-80,631,300 , GRCh37.p13 chr5: 79,816,220-79,927,119 ANKRD34B, DHFR, 3 more genes
    nsv6768162copy number variation1nstd229human GRCh38 chr5: 80,619,256-80,773,851 , GRCh37.p13 chr5: 79,915,075-80,069,670 DHFR, LINC01337, 2 more genes
    nsv6767907copy number variation1nstd229human GRCh38 chr5: 80,631,411-80,670,883 , GRCh37.p13 chr5: 79,927,230-79,966,702 DHFR, MTRNR2L2, 1 more genes
    nsv6760524copy number variation1nstd229human GRCh38 chr5: 80,599,801-80,690,800 , GRCh37.p13 chr5: 79,895,620-79,986,619 MSH3, MTRNR2L2, 3 more genes
    nsv6562791inversion1nstd223human GRCh38 chr5: 80,630,036-80,630,608 , GRCh37.p13 chr5: 79,925,855-79,926,427 DHFR
    nsv6408426copy number variation1nstd223human GRCh38 chr5: 80,633,400-80,638,499 , GRCh37.p13 chr5: 79,929,219-79,934,318 DHFR
    nsv6312304copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,929,676-79,966,148 , GRCh38.p12 chr5: 80,633,857-80,670,329 DHFR, MSH3, 1 more genes
    nsv6312212copy number variation1nstd102humanPathogenic GRCh37 chr5: 79,949,868-80,064,832 , GRCh38.p12 chr5: 80,654,049-80,769,013 MSH3, DHFR
    nsv6312118copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,950,537-80,171,691 , GRCh38.p12 chr5: 80,654,718-80,875,872 RPS26P27, DHFR, 1 more genes
    nsv6312008copy number variation1nstd102humanUncertain significance GRCh37 chr5: 79,949,868-80,109,570 , GRCh38.p12 chr5: 80,654,049-80,813,751 MSH3, DHFR
    nsv6244437mobile element insertion1nstd215human GRCh38 chr5: 80,630,764-80,630,764 , GRCh37.p13 chr5: 79,926,583-79,926,583 DHFR
    nsv6135683copy number variation1nstd213human GRCh37 chr5: 76,940,000-80,890,001 , GRCh38.p12 chr5: 77,644,175-81,594,182 ACTBP2, ARSB, 63 more genes
    nsv6135437copy number variation1nstd213human GRCh37 chr5: 78,580,000-80,500,001 , GRCh38.p12 chr5: 79,284,177-81,204,182 DBIP2, DHFR, 40 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
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