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Items: 1 to 20 of 217

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv7061355inversion1nstd229human GRCh38 chr9: 28,756,551-29,044,685 , GRCh37.p13 chr9: 28,756,549-29,044,683 LINGO2, MIR876, 1 more genes
    nsv6877750copy number variation1nstd229human GRCh38 chr9: 28,879,963-28,891,169 , GRCh37.p13 chr9: 28,879,961-28,891,167 MIR873, LINGO2
    nsv6877158copy number variation1nstd229human GRCh38 chr9: 28,846,901-28,893,800 , GRCh37.p13 chr9: 28,846,899-28,893,798 MIR876, LINGO2, 1 more genes
    nsv6876377copy number variation1nstd229human GRCh38 chr9: 28,807,248-28,914,469 , GRCh37.p13 chr9: 28,807,246-28,914,467 MIR873, LINGO2, 1 more genes
    nsv6875942copy number variation1nstd229human GRCh38 chr9: 24,741,564-30,889,392 , GRCh37.p13 chr9: 24,741,562-30,889,390 IFNK, LINC01242, 46 more genes
    nsv6874920copy number variation1nstd229human GRCh38 chr9: 28,648,931-28,997,273 , GRCh37.p13 chr9: 28,648,929-28,997,271 MIR873, MIR876, 2 more genes
    nsv6869660copy number variation1nstd229human GRCh38 chr9: 28,612,601-28,951,300 , GRCh37.p13 chr9: 28,612,599-28,951,298 LINGO2, MIR876, 2 more genes
    nsv6868104copy number variation1nstd229human GRCh38 chr9: 28,868,356-28,929,212 , GRCh37.p13 chr9: 28,868,354-28,929,210 LINGO2, MIR873
    nsv6867828copy number variation1nstd229human GRCh38 chr9: 28,850,401-28,907,300 , GRCh37.p13 chr9: 28,850,399-28,907,298 LINGO2, MIR876, 1 more genes
    nsv6867427copy number variation1nstd229human GRCh38 chr9: 28,852,094-29,025,112 , GRCh37.p13 chr9: 28,852,092-29,025,110 MIR876, MIR873, 1 more genes
    nsv6867417copy number variation1nstd229human GRCh38 chr9: 28,644,078-28,953,683 , GRCh37.p13 chr9: 28,644,076-28,953,681 MIR876, LINGO2, 2 more genes
    nsv6866643copy number variation1nstd229human GRCh38 chr9: 28,859,322-28,913,141 , GRCh37.p13 chr9: 28,859,320-28,913,139 LINGO2, MIR876, 1 more genes
    nsv6863268copy number variation1nstd229human GRCh38 chr9: 28,771,607-28,999,607 , GRCh37.p13 chr9: 28,771,605-28,999,605 MIR876, LINGO2, 1 more genes
    nsv6861923copy number variation1nstd229human GRCh38 chr9: 28,660,301-28,962,100 , GRCh37.p13 chr9: 28,660,299-28,962,098 LINGO2, MIR876, 1 more genes
    nsv6861659copy number variation1nstd229human GRCh38 chr9: 28,772,223-28,964,684 , GRCh37.p13 chr9: 28,772,221-28,964,682 LINGO2, MIR876, 1 more genes
    nsv6859940copy number variation1nstd229human GRCh38 chr9: 28,764,214-29,163,955 , GRCh37.p13 chr9: 28,764,212-29,163,953 LINGO2, MIR876, 1 more genes
    nsv6637770copy number variation1nstd102humanUncertain significance GRCh37 chr9: 27,257,570-31,635,608 , GRCh38.p12 chr9: 27,257,572-31,635,610 LOC105376002, CDRT15P5, 32 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6634409copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 1-40,036,525 , GRCh38.p12 chr9: 10,001-39,445,729 ACO1, PLIN2, 594 more genes
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