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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6896058copy number variation1nstd229human GRCh38 chr10: 91,896,434-91,905,284 , GRCh37.p13 chr10: 93,656,191-93,665,041 FGFBP3
    nsv6886062copy number variation1nstd229human GRCh38 chr10: 91,870,968-91,981,432 , GRCh37.p13 chr10: 93,630,725-93,741,189 FGFBP3, BTAF1
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637584copy number variation1nstd102humanUncertain significance GRCh37 chr10: 93,577,943-93,922,822 , GRCh38.p12 chr10: 91,818,186-92,163,065 EIF4A1P8, CPEB3, 5 more genes
    nsv6620929copy number variation1nstd224human GRCh37 chr10: 93,412,994-94,014,958 , GRCh38.p12 chr10: 91,653,237-92,255,201 EIF4A1P8, LOC107984253, 11 more genes
    nsv6132059copy number variation1nstd213human GRCh37 chr10: 93,460,000-93,770,001 , GRCh38.p12 chr10: 91,700,243-92,010,244 BTAF1, TNKS2, 5 more genes
    nsv5921993copy number variation1nstd209human GRCh38 chr10: 90,979,234-99,692,336 , GRCh37.p13 chr10: 92,738,991-101,452,093 , CYP2C115P, 166 more genes
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4616183copy number variation1nstd183human GRCh37 chr10: 93,668,098-93,668,730 , GRCh38.p12 chr10: 91,908,341-91,908,973 FGFBP3
    nsv4426084copy number variation1nstd174human GRCh37 chr10: 93,668,098-93,668,730 , GRCh38.p12 chr10: 91,908,341-91,908,973 FGFBP3
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4325673inversion1nstd166human GRCh37.p13 chr10: 92,228,734-107,785,320 , GRCh38.p12 chr10: 90,468,977-106,025,562 , COX15, 323 more genes
    nsv3920295copy number variation1nstd102humanPathogenic NCBI36 chr10: 81,675,342-135,374,737 , GRCh37.p13 chr10: 81,685,362-135,524,747 , GRCh38.p12 chr10: 79,925,606-133,787,422 EIF2S2P3, CYP17A1-AS1, 895 more genes
    nsv3909746copy number variation1nstd102humanBenign GRCh37 chr10: 93,668,341-93,668,663 , GRCh38.p12 chr10: 91,908,584-91,908,906 FGFBP3
    nsv3908115copy number variation1nstd102humanPathogenic GRCh37 chr10: 92,667,881-98,970,384 , GRCh38.p12 chr10: 90,908,124-97,210,627 EXOC6, MARCHF5, 118 more genes
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