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Items: 1 to 20 of 495

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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
    nsv7070433inversion1nstd229human GRCh38 chr15: 28,680,335-30,817,180 , GRCh37.p13 chr15: 28,925,481-31,109,383 RNU6-17P, RN7SL628P, 54 more genes
    nsv7068342inversion1nstd229human GRCh38 chr15: 29,120,877-31,530,094 , GRCh37.p13 chr15: 29,413,080-31,822,297 ULK4P2, TRPM1, 57 more genes
    nsv7065318inversion1nstd229human GRCh38 chr15: 29,942,582-32,138,315 , GRCh37.p13 chr15: 30,234,785-32,430,516 GOLGA8T, ARHGAP11B, 52 more genes
    nsv7061220inversion1nstd229human GRCh38 chr15: 28,848,197-32,920,244 , GRCh37.p13 chr15: 29,093,343-33,212,445 LOC105376704, WHAMMP1, 96 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
    nsv6637612copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,934,987-30,386,399 , GRCh38.p12 chr15: 28,689,841-30,094,196 , GRCh38.p12 chr15|NW_011332701.1: 851,845-2,266,916 , GRCh38.p12 chr15|NT_187660.1: 965,631-2,379,400 RN7SL719P, LOC100129687, 21 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
    nsv6637571copy number variation1nstd102humanUncertain significance GRCh37 chr15: 29,211,751-30,386,553 , GRCh38.p12 chr15: 28,919,548-30,094,350 , GRCh38.p12 chr15|NT_187660.1: 1,194,503-2,379,554 , GRCh38.p12 chr15|NW_011332701.1: 1,082,019-2,267,070 ENTREP2, LOC105370743, 11 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
    nsv6637528copy number variation1nstd102humanPathogenic GRCh37 chr15: 30,370,018-32,446,830 , GRCh38.p12 chr15: 30,077,815-32,154,629 OTUD7A, LOC105370752, 49 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
    nsv6637375copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,928,730-30,386,398 , GRCh38.p12 chr15: 28,683,584-30,094,195 , GRCh38.p12 chr15|NT_187660.1: 959,374-2,379,399 , GRCh38.p12 chr15|NW_011332701.1: 845,588-2,266,915 LOC107984746, NCAPGP2, 22 more genes
    nsv6637197copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,540,415-32,446,830 , GRCh38.p12 chr15: 28,295,269-32,154,629 RN7SL238P, DEPDC1P1, 90 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
    nsv6623094copy number variation1nstd224human GRCh37 chr15: 30,053,418-30,665,181 , GRCh38.p12 chr15: 29,761,215-30,372,978 ULK4P3, DNM1P30, 14 more genes
    nsv6595355inversion1nstd223human GRCh38 chr15: 28,146,412-30,832,660 , GRCh37.p13 chr15: 28,391,558-31,124,863 CHRFAM7A, RN7SL673P, 73 more genes
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