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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
    nsv6637553copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-30,386,553 , GRCh38.p12 chr15: 23,319,714-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 FAN1, LOC105370751, 247 more genes
    nsv6637399copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,355 , GRCh38.p12 chr15: 23,319,714-28,300,209 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 DNM1P28, MIR4508, 246 more genes
    nsv6634429copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,739,497-28,566,579 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 20,534,259-28,321,433 OR11J7P, SNORD115-21, 364 more genes
    nsv6315545copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,862-28,522,838 , GRCh38.p12 chr15: 23,319,714-28,277,692 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SERPINE4P, SNORD116-30, 246 more genes
    nsv6315542copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,285,775-30,386,399 , GRCh38.p12 chr15: 23,319,714-30,094,196 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 RPL5P1, SNORD115-11, 247 more genes
    nsv6315525copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-29,855,014 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-29,562,810 SNORD115-37, LOC105376704, 247 more genes
    nsv6315485copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-28,635,058 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,389,912 SNORD116-28, MPHOSPH10P8, 247 more genes
    nsv6315479copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,288,374-28,534,245 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,289,099 OTUD7A, HMGN2P5, 246 more genes
    nsv6315473copy number variation1nstd102humanUncertain significance GRCh37 chr15: 22,770,421-29,057,676 , GRCh38.p12 chr15: 23,319,714-28,812,530 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 CHRFAM7A, DNM1P29, 247 more genes
    nsv6314960copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,780,392-32,784,132 , GRCh38.p12 chr15|NW_011332701.1: 697,255-4,544,070 , GRCh38.p12 chr15: 28,535,246-32,491,931 , GRCh38.p12 chr15|NT_187660.1: 811,041-4,593,906 TJP1, LOC107984779, 97 more genes
    nsv6132889copy number variation1nstd213human GRCh37 chr15: 29,700,000-30,660,001 , GRCh38.p12 chr15: 29,407,796-30,367,798 , GRCh38.p12 chr15|NT_187660.1: 1,683,295-2,652,773 , GRCh38.p12 chr15|NW_011332701.1: 1,570,811-2,540,289 LINC02249, GOLGA8J, 21 more genes
    nsv6130428insertion1nstd186human GRCh37 chr15: 30,465,469-30,465,529 , GRCh38.p12 chr15: 30,173,266-30,173,326 , GRCh38.p12 chr15|NT_187660.1: 2,458,214-2,458,274 , GRCh38.p12 chr15|NW_011332701.1: 2,345,730-2,345,790 LOC105370746
    nsv6130335insertion1nstd186human GRCh37 chr15: 30,465,464-30,465,551 , GRCh38.p12 chr15|NW_011332701.1: 2,345,725-2,345,812 , GRCh38.p12 chr15: 30,173,261-30,173,348 , GRCh38.p12 chr15|NT_187660.1: 2,458,209-2,458,296 LOC105370746
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
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