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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148130copy number variation1nstd102humanPathogenic GRCh37 chr8: 36,763,176-50,929,707 , GRCh38.p12 chr8: 36,905,658-50,017,147 SNTG1, RN7SL806P, 193 more genes
    nsv7098173copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,117,538-38,961,219 , GRCh38.p12 chr8: 38,260,020-39,103,700 TM2D2, FGFR1, 14 more genes
    nsv6842461copy number variation1nstd229human GRCh38 chr8: 38,988,364-38,988,410 , GRCh37.p13 chr8: 38,845,883-38,845,929 HTRA4, TM2D2
    nsv6839650copy number variation1nstd229human GRCh38 chr8: 38,572,201-41,442,522 , GRCh37.p13 chr8: 38,429,719-41,300,041 RPL3P10, SNORD65B, 35 more genes
    nsv6634301complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,132,174 , GRCh37 chr8: 158,048-42,987,317 NAT1, NAT2, 758 more genes
    nsv6632982copy number variation1nstd224human GRCh37 chr8: 38,762,056-39,892,501 , GRCh38.p12 chr8: 38,904,538-40,034,982 , GRCh38.p12 chr8|NT_187577.1: 1-624,492 ADAM9, SNORD38D, 15 more genes
    nsv6561497inversion1nstd223human GRCh38 chr8: 38,983,536-38,984,031 , GRCh37.p13 chr8: 38,841,055-38,841,550 HTRA4
    nsv6419646copy number variation1nstd223human GRCh38 chr8: 38,982,101-38,984,300 , GRCh37.p13 chr8: 38,839,620-38,841,819 HTRA4
    nsv6315323complex substitution1nstd102humanPathogenic GRCh38.p12 chr8: 208,048-43,164,161 , GRCh37 chr8: 158,048-43,019,304 NAT1, NAT2, 760 more genes
    nsv6313822copy number variation1nstd102humanUncertain significance GRCh37 chr8: 38,430,146-41,294,984 , GRCh38.p12 chr8: 38,572,628-41,437,465 RNU6-895P, ADAM9, 35 more genes
    nsv6312909copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr8: 37,595,441-38,961,219 , GRCh38.p12 chr8: 37,737,923-39,103,700 LSM1, BAG4, 33 more genes
    nsv6245889mobile element insertion1nstd215human GRCh38 chr8: 38,982,524-38,982,524 , GRCh37.p13 chr8: 38,840,043-38,840,043 HTRA4
    nsv6136674copy number variation1nstd213human GRCh37 chr8: 38,810,000-39,050,001 , GRCh38.p12 chr8: 38,952,482-39,192,482 ADAM9, PLEKHA2, 5 more genes
    nsv6136579copy number variation1nstd213human GRCh37 chr8: 38,200,000-38,900,001 , GRCh38.p12 chr8: 38,342,482-39,042,482 FGFR1, ADAM9, 12 more genes
    nsv6136043copy number variation1nstd213human GRCh37 chr8: 38,540,000-38,980,001 , GRCh38.p12 chr8: 38,682,482-39,122,482 TACC1, ADAM9, 5 more genes
    nsv6136042copy number variation1nstd213human GRCh37 chr8: 38,160,000-38,880,001 , GRCh38.p12 chr8: 38,302,482-39,022,482 PLEKHA2, TM2D2, 12 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5116884mobile element insertion1nstd203human GRCh38 chr8: 38,977,265-38,977,282 , GRCh37.p13 chr8: 38,834,784-38,834,801 HTRA4
    nsv5109716mobile element insertion1nstd203human GRCh38 chr8: 38,976,322-38,976,332 , GRCh37.p13 chr8: 38,833,841-38,833,851 HTRA4
    nsv5102883mobile element insertion1nstd203human GRCh38 chr8: 38,977,267-38,977,282 , GRCh37.p13 chr8: 38,834,786-38,834,801 HTRA4
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