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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5696155mobile element insertion2nstd211human GRCh38 chr13: 73,074,400-73,074,400 , GRCh37.p13 chr13: 73,648,538-73,648,538 KLF5
    nsv5655748insertion1nstd207human GRCh38 chr13: 73,074,381-73,074,381 , GRCh37.p13 chr13: 73,648,519-73,648,519 KLF5
    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
    nsv5513527copy number variation1nstd206human GRCh38 chr13: 73,069,996-73,070,182 , GRCh37.p13 chr13: 73,644,134-73,644,320 KLF5
    nsv5511482copy number variation1nstd206human GRCh38 chr13: 73,075,233-73,075,299 , GRCh37.p13 chr13: 73,649,371-73,649,437 KLF5
    nsv5419793mobile element insertion1nstd206human GRCh38 chr13: 73,074,381-73,074,381 , GRCh37.p13 chr13: 73,648,519-73,648,519 KLF5
    nsv5144920mobile element insertion1nstd203human GRCh38 chr13: 73,074,385-73,074,400 , GRCh37.p13 chr13: 73,648,523-73,648,538 KLF5
    nsv5143297mobile element insertion1nstd203human GRCh38 chr13: 73,074,381-73,074,400 , GRCh37.p13 chr13: 73,648,519-73,648,538 KLF5
    nsv5034873inversion1nstd200human GRCh38 chr13: 55,150,893-76,780,363 , GRCh37.p13 chr13: 55,725,028-77,354,498 , PRR20C, 199 more genes
    nsv5033445inversion1nstd200human GRCh38 chr13: 63,639,797-112,722,344 , GRCh37.p13 chr13: 64,213,930-113,376,658 , RPL15P18, 564 more genes
    nsv4872325inversion1nstd200human GRCh37 chr13: 55,725,028-77,354,498 , GRCh38.p12 chr13: 55,150,893-76,780,363 , OR7E111P, 199 more genes
    nsv4871044inversion1nstd200human GRCh37 chr13: 64,213,930-113,376,658 , GRCh38.p12 chr13: 63,639,797-112,722,344 , TUBGCP3, 564 more genes
    nsv4675995copy number variation1nstd102humanPathogenic GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857 RNU7-88P, LINC00564, 396 more genes
    nsv4675850copy number variation1nstd102humanPathogenic GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258 TEX30, LOC101927712, 680 more genes
    nsv4675244copy number variation1nstd102humanPathogenic GRCh37 chr13: 71,502,357-86,571,730 , GRCh38.p12 chr13: 70,928,225-85,997,595 RNU6-79P, LINC01069, 151 more genes
    nsv4675016copy number variation1nstd102humanUncertain significance GRCh37 chr13: 58,432,035-73,649,333 , GRCh38.p12 chr13: 57,857,901-73,075,195 TRIM60P19, ATXN8OS, 137 more genes
    nsv4611519copy number variation2nstd183human GRCh37 chr13: 73,632,682-73,634,039 , GRCh38.p12 chr13: 73,058,544-73,059,901 KLF5
    nsv4552193insertion1nstd166human GRCh37.p13 chr13: 73,648,519-73,648,519 , GRCh38.p12 chr13: 73,074,381-73,074,381 KLF5
    nsv4456561copy number variation1nstd102humanPathogenic GRCh37 chr13: 61,775,567-115,107,733 , GRCh38.p12 chr13: 61,201,433-114,342,258 LOC105370262, LINC01080, 609 more genes
    nsv4371018copy number variation1nstd173human GRCh37 chr13: 73,577,966-73,701,559 , GRCh38.p12 chr13: 73,003,828-73,127,422 RNU6-66P, PIBF1, 3 more genes
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