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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129759insertion1nstd186human GRCh37 chr13: 25,154,718-25,154,741 , GRCh38.p12 chr13: 24,580,580-24,580,603 TPTE2P6
    nsv5941905copy number variation1nstd209human GRCh38 chr13: 24,586,531-24,602,932 , GRCh37.p13 chr13: 25,160,669-25,177,070 TPTE2P6
    nsv5937357copy number variation1nstd209human GRCh38 chr13: 24,558,458-24,762,880 , GRCh37.p13 chr13: 25,132,596-25,337,018 , ANKRD20A10P, 11 more genes
    nsv5930119copy number variation1nstd209human GRCh38 chr13: 19,425,704-24,953,999 , GRCh37.p13 chr13: 19,999,844-25,528,137 , LOC105370102, 128 more genes
    nsv5860202copy number variation2nstd209human GRCh38 chr13: 24,586,748-24,603,850 , GRCh37.p13 chr13: 25,160,886-25,177,988 TPTE2P6
    nsv5858558copy number variation2nstd209human GRCh38 chr13: 24,588,571-24,593,229 , GRCh37.p13 chr13: 25,162,709-25,167,367 TPTE2P6
    nsv5858533copy number variation1nstd209human GRCh38 chr13: 24,597,478-24,614,946 , GRCh37.p13 chr13: 25,171,616-25,189,084 LOC107984610, TPTE2P6
    nsv5850427copy number variation1nstd209human GRCh38 chr13: 24,558,483-24,586,347 , GRCh37.p13 chr13: 25,132,621-25,160,485 PSPC1P2, LOC101927375, 1 more genes
    nsv5847926copy number variation2nstd209human GRCh38 chr13: 24,582,965-24,584,214 , GRCh37.p13 chr13: 25,157,103-25,158,352 TPTE2P6
    nsv5729970mobile element insertion1nstd211human GRCh38 chr13: 24,582,066-24,582,066 , GRCh37.p13 chr13: 25,156,204-25,156,204 TPTE2P6
    nsv5658602insertion1nstd207human GRCh38 chr13: 24,580,552-24,580,552 , GRCh37.p13 chr13: 25,154,690-25,154,690 TPTE2P6
    nsv5653899insertion1nstd207human GRCh38 chr13: 24,595,891-24,595,891 , GRCh37.p13 chr13: 25,170,029-25,170,029 TPTE2P6
    nsv5598279copy number variation1nstd207human GRCh38 chr13: 24,586,531-24,602,932 , GRCh37.p13 chr13: 25,160,669-25,177,070 TPTE2P6
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561491sequence alteration1nstd206human GRCh38 chr13: 24,595,804-24,953,333 , GRCh37.p13 chr13: 25,169,942-25,527,471 , ATP12A, 13 more genes
    nsv5560874mobile element insertion1nstd206human GRCh38 chr13: 24,582,066-24,582,070 , GRCh37.p13 chr13: 25,156,204-25,156,208 TPTE2P6
    nsv5546921insertion1nstd206human GRCh38 chr13: 24,580,580-24,580,603 , GRCh37.p13 chr13: 25,154,718-25,154,741 TPTE2P6
    nsv5509932copy number variation1nstd206human GRCh38 chr13: 24,586,539-24,602,956 , GRCh37.p13 chr13: 25,160,677-25,177,094 TPTE2P6
    nsv5505776copy number variation1nstd206human GRCh38 chr13: 24,588,000-24,672,106 , GRCh37.p13 chr13: 25,162,138-25,246,244 TPTE2P6, LOC107984610
    nsv5392866copy number variation2nstd186human GRCh37 chr13: 25,160,705-25,177,071 , GRCh38.p12 chr13: 24,586,567-24,602,933 TPTE2P6
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