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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
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7098698complex chromosomal rearrangement11nstd230human GRCh37 chr3: 93,803,158-93,803,158 , GRCh37 chr3: 93,803,166-93,803,166 , GRCh37 chr3: 167,331,870-167,331,870 , GRCh37 chr3: 167,331,870-167,331,870 , GRCh37 chr3: 167,468,898-167,468,898 , GRCh37 chr3: 167,468,902-167,468,902 , GRCh37 chr3: 167,469,070-167,469,070 , GRCh37 chr3: 167,559,279-167,559,279 , GRCh37 chr3: 167,578,509-167,578,509 , GRCh37 chr3: 167,579,292-167,579,292 , GRCh37 chr3: 167,581,705-167,581,705 , GRCh37 chr3: 167,581,705-167,581,705 , GRCh37 chr3: 171,061,627-171,061,627 , GRCh37 chr3: 171,061,627-171,061,627 , GRCh37 chr10: 122,874,516-122,874,516 , GRCh37 chr10: 122,874,523-122,874,523 , GRCh37 chr10: 122,922,817-122,922,817 , GRCh37 chr10: 122,922,818-122,922,818 , GRCh37 chr11: 20,842,931-20,842,931 , GRCh37 chr11: 20,842,936-20,842,936 , GRCh37 chr11: 20,878,690-20,878,690 , GRCh37 chr11: 20,878,693-20,878,693 , GRCh38.p12 chr10: 121,115,002-121,115,002 , GRCh38.p12 chr10: 121,115,009-121,115,009 , GRCh38.p12 chr10: 121,163,303-121,163,303 , GRCh38.p12 chr10: 121,163,304-121,163,304 , GRCh38.p12 chr11: 20,821,385-20,821,385 , GRCh38.p12 chr11: 20,821,390-20,821,390 , GRCh38.p12 chr11: 20,857,144-20,857,144 , GRCh38.p12 chr11: 20,857,147-20,857,147 , GRCh38.p12 chr3: 94,084,314-94,084,314 , GRCh38.p12 chr3: 94,084,322-94,084,322 , GRCh38.p12 chr3: 167,614,082-167,614,082 , GRCh38.p12 chr3: 167,614,082-167,614,082 , GRCh38.p12 chr3: 167,751,110-167,751,110 , GRCh38.p12 chr3: 167,751,114-167,751,114 , GRCh38.p12 chr3: 167,751,282-167,751,282 , GRCh38.p12 chr3: 167,841,491-167,841,491 , GRCh38.p12 chr3: 167,860,721-167,860,721 , GRCh38.p12 chr3: 167,861,504-167,861,504 , GRCh38.p12 chr3: 167,863,917-167,863,917 , GRCh38.p12 chr3: 167,863,917-167,863,917 , GRCh38.p12 chr3: 171,343,838-171,343,838 , GRCh38.p12 chr3: 171,343,838-171,343,838 NELL1, SERPINI1, 3 more genes
    nsv7096968copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,772,011-93,845,334 , GRCh38.p12 chr3: 94,053,167-94,126,490 ARL13B, RBBP4P2, 2 more genes
    nsv7056776inversion1nstd229human GRCh38 chr3: 94,108,447-94,108,662 , GRCh37.p13 chr3: 93,827,291-93,827,506 NSUN3
    nsv7042107inversion1nstd229human GRCh38 chr3: 94,077,966-94,083,730 , GRCh37.p13 chr3: 93,796,810-93,802,574 NSUN3
    nsv7041727inversion1nstd229human GRCh38 chr3: 94,070,424-99,088,195 , GRCh37.p13 chr3: 93,789,268-98,807,039 LINC00973, OR5H7P, 63 more genes
    nsv6717354copy number variation1nstd229human GRCh38 chr3: 94,093,413-94,096,879 , GRCh37.p13 chr3: 93,812,257-93,815,723 NSUN3
    nsv6717045copy number variation1nstd229human GRCh38 chr3: 94,108,346-94,113,916 , GRCh37.p13 chr3: 93,827,190-93,832,760 NSUN3
    nsv6710585copy number variation1nstd229human GRCh38 chr3: 94,117,472-94,122,821 , GRCh37.p13 chr3: 93,836,316-93,841,665 NSUN3
    nsv6707693copy number variation1nstd229human GRCh38 chr3: 94,068,624-94,071,325 , GRCh37.p13 chr3: 93,787,468-93,790,169 NSUN3
    nsv6706870copy number variation1nstd229human GRCh38 chr3: 94,122,860-94,123,027 , GRCh37.p13 chr3: 93,841,704-93,841,871 NSUN3
    nsv6706371copy number variation1nstd229human GRCh38 chr3: 94,083,491-94,086,606 , GRCh37.p13 chr3: 93,802,335-93,805,450 NSUN3
    nsv6702528copy number variation1nstd229human GRCh38 chr3: 94,089,686-94,093,350 , GRCh37.p13 chr3: 93,808,530-93,812,194 NSUN3
    nsv6700476copy number variation1nstd229human GRCh38 chr3: 94,060,298-94,064,252 , GRCh37.p13 chr3: 93,779,142-93,783,096 DHFR2, NSUN3
    nsv6636560copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 93,519,465-94,372,131 , GRCh38.p12 chr3: 93,800,621-94,653,287 PROS1, NSUN3, 10 more genes
    nsv6629324copy number variation1nstd224human GRCh37 chr3: 93,593,119-94,679,788 , GRCh38.p12 chr3: 93,874,275-94,960,944 NSUN3, DHFR2, 11 more genes
    nsv6536115inversion1nstd223human GRCh38 chr3: 94,085,786-94,086,213 , GRCh37.p13 chr3: 93,804,630-93,805,057 NSUN3
    nsv6375012copy number variation1nstd223human GRCh38 chr3: 94,093,413-94,096,879 , GRCh37.p13 chr3: 93,812,257-93,815,723 NSUN3
    nsv6374651copy number variation1nstd223human GRCh38 chr3: 94,060,981-94,061,476 , GRCh37.p13 chr3: 93,779,825-93,780,320 DHFR2, NSUN3
    nsv6368438copy number variation1nstd223human GRCh38 chr3: 94,089,685-94,096,879 , GRCh37.p13 chr3: 93,808,529-93,815,723 NSUN3
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