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Items: 1 to 20 of 179

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138236copy number variation1nstd232human GRCh37.p13 chr7: 100,853,724-100,853,810 , GRCh38.p12 chr7: 101,210,443-101,210,529 PLOD3
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7097852copy number variation1nstd102humanUncertain significance GRCh37 chr7: 100,853,354-100,860,555 , GRCh38.p12 chr7: 101,210,073-101,217,274 PLOD3, ZNHIT1
    nsv7097466copy number variation1nstd102humanUncertain significance GRCh37 chr7: 100,852,114-100,860,555 , GRCh38.p12 chr7: 101,208,833-101,217,274 PLOD3, ZNHIT1
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7051497inversion1nstd229human GRCh38 chr7: 100,869,983-101,245,444 , GRCh37.p13 chr7: 100,467,605-100,888,725 MUC12, FIS1, 23 more genes
    nsv6837371copy number variation1nstd229human GRCh38 chr7: 101,140,119-101,283,888 , GRCh37.p13 chr7: 100,783,400-100,927,169 MOGAT3, PLOD3, 10 more genes
    nsv6837075copy number variation1nstd229human GRCh38 chr7: 101,209,793-101,231,514 , GRCh37.p13 chr7: 100,853,074-100,874,795 ZNHIT1, CLDN15, 1 more genes
    nsv6832160copy number variation1nstd229human GRCh38 chr7: 101,200,205-101,210,191 , GRCh37.p13 chr7: 100,843,486-100,853,472 MOGAT3, DGAT2L7P, 2 more genes
    nsv6826957copy number variation1nstd229human GRCh38 chr7: 100,918,010-102,186,129 , GRCh37.p13 chr7: 100,515,630-101,718,950 COL26A1, AP1S1, 28 more genes
    nsv6820511copy number variation1nstd229human GRCh38 chr7: 100,411,473-102,072,572 , GRCh37.p13 chr7: 100,009,096-101,715,852 MIR4653, UFSP1, 63 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6614776copy number variation1nstd223human GRCh38 chr7: 99,943,801-101,566,300 , GRCh37.p13 chr7: 99,541,424-101,209,580 MUC12, FBXO24, 95 more genes
    nsv6613156copy number variation1nstd223human GRCh38 chr7: 101,195,311-101,207,130 , GRCh37.p13 chr7: 100,838,592-100,850,411 PLOD3, DGAT2L7P, 2 more genes
    nsv6609864copy number variation1nstd223human GRCh38 chr7: 101,204,773-101,205,657 , GRCh37.p13 chr7: 100,848,054-100,848,938 RPSAP46, PLOD3
    nsv6604708copy number variation1nstd223human GRCh38 chr7: 100,460,230-101,238,868 , GRCh37.p13 chr7: 100,057,853-100,882,149 RN7SKP54, ZNHIT1, 49 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6313503copy number variation1nstd102humanPathogenic GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253 GJC3, LAMB4, 237 more genes
    nsv6312516copy number variation1nstd102humanUncertain significance GRCh37 chr7: 100,849,562-100,850,205 , GRCh38.p12 chr7: 101,206,281-101,206,924 PLOD3
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