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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7015873copy number variation1nstd229human GRCh38 chr18: 35,479,292-35,697,767 , GRCh37.p13 chr18: 33,059,256-33,277,731 LOC105372065, GALNT1, 3 more genes
    nsv7011566copy number variation1nstd229human GRCh38 chr18: 35,492,101-35,505,200 , GRCh37.p13 chr18: 33,072,065-33,085,164 INO80C
    nsv7010412copy number variation1nstd229human GRCh38 chr18: 35,456,877-35,715,407 , GRCh37.p13 chr18: 33,036,841-33,295,371 LOC105372065, GALNT1, 3 more genes
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7007093copy number variation1nstd229human GRCh38 chr18: 35,471,058-35,473,126 , GRCh37.p13 chr18: 33,051,022-33,053,090 INO80C
    nsv6531154copy number variation1nstd223human GRCh38 chr18: 35,439,853-36,067,571 , GRCh37.p13 chr18: 33,019,817-33,647,534 LOC105372066, MIR187, 9 more genes
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6259345mobile element insertion1nstd215human GRCh38 chr18: 35,478,273-35,478,273 , GRCh37.p13 chr18: 33,058,237-33,058,237 INO80C
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133334copy number variation1nstd213human GRCh37 chr18: 32,810,000-34,010,001 , GRCh38.p12 chr18: 35,230,036-36,430,038 GALNT1, ZNF24, 23 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6107779inversion1nstd212human GRCh38 chr18: 34,743,532-36,146,243 , GRCh37.p13 chr18: 32,323,496-33,726,206 , DTNA, 22 more genes
    nsv5710161mobile element insertion2nstd211human GRCh38 chr18: 35,475,906-35,475,906 , GRCh37.p13 chr18: 33,055,870-33,055,870 INO80C
    nsv5561206mobile element insertion1nstd206human GRCh38 chr18: 35,496,831-35,496,831 , GRCh37.p13 chr18: 33,076,795-33,076,795 INO80C
    nsv5532113copy number variation1nstd206human GRCh38 chr18: 35,471,018-35,471,163 , GRCh37.p13 chr18: 33,050,982-33,051,127 INO80C
    nsv5423922mobile element insertion1nstd206human GRCh38 chr18: 35,475,906-35,475,957 , GRCh37.p13 chr18: 33,055,870-33,055,921 INO80C
    nsv5374933translocation1nstd200human GRCh38 chr18: 35,498,379-35,498,379 , GRCh38 chr17: 44,078,294-44,078,294 , GRCh37.p13 chr17: 42,155,662-42,155,662 , GRCh37.p13 chr18: 33,078,343-33,078,343 HDAC5, INO80C
    nsv5155280mobile element insertion1nstd203human GRCh38 chr18: 35,475,904-35,475,906 , GRCh37.p13 chr18: 33,055,868-33,055,870 INO80C
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