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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7147425copy number variation1nstd232human GRCh37.p13 chr7: 100,275,282-100,275,372 , GRCh38.p12 chr7: 100,677,659-100,677,749 GNB2, GIGYF1
    nsv7140356copy number variation1nstd232human GRCh37.p13 chr7: 100,276,234-100,276,313 , GRCh38.p12 chr7: 100,678,611-100,678,690 GNB2, GIGYF1
    nsv7138095copy number variation1nstd232human GRCh37.p13 chr7: 100,275,922-100,276,019 , GRCh38.p12 chr7: 100,678,299-100,678,396 GNB2, GIGYF1
    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
    nsv7055390inversion1nstd229human GRCh38 chr7: 100,184,977-102,400,588 , GRCh37.p13 chr7: 99,782,600-101,718,950 SLC12A9-AS1, STAG3, 84 more genes
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv7051377inversion1nstd229human GRCh38 chr7: 100,664,103-100,724,101 , GRCh37.p13 chr7: 100,261,726-100,321,724 EPO, GNB2, 3 more genes
    nsv7045773inversion1nstd229human GRCh38 chr7: 100,499,070-100,696,514 , GRCh37.p13 chr7: 100,096,693-100,294,137 AGFG2, LOC105375429, 13 more genes
    nsv6837767copy number variation1nstd229human GRCh38 chr7: 100,603,658-100,679,521 , GRCh37.p13 chr7: 100,201,281-100,277,144 PCOLCE-AS1, LOC105375429, 6 more genes
    nsv6822884copy number variation1nstd229human GRCh38 chr7: 100,573,701-100,682,700 , GRCh37.p13 chr7: 100,171,324-100,280,323 PCOLCE-AS1, GIGYF1, 9 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
    nsv6818312copy number variation1nstd229human GRCh38 chr7: 100,547,001-100,919,000 , GRCh37.p13 chr7: 100,144,624-100,516,620 TRIP6, MIR6875, 24 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
    nsv6610980copy number variation1nstd223human GRCh38 chr7: 100,548,101-100,840,100 , GRCh37.p13 chr7: 100,145,724-100,437,722 LRCH4, MOSPD3, 18 more genes
    nsv6607668copy number variation1nstd223human GRCh38 chr7: 100,428,001-100,907,900 , GRCh37.p13 chr7: 100,025,624-100,505,520 LOC107986829, FBXO24, 33 more genes
    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
    nsv6601439copy number variation1nstd223human GRCh38 chr7: 100,412,401-100,918,900 , GRCh37.p13 chr7: 100,010,024-100,516,520 TSC22D4, NYAP1, 33 more genes
    nsv6565919inversion1nstd223human GRCh38 chr7: 100,671,952-100,672,002 , GRCh37.p13 chr7: 100,269,575-100,269,625 GNB2
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