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Items: 1 to 20 of 108

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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
    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
    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
    nsv6374651copy number variation1nstd223human GRCh38 chr3: 94,060,981-94,061,476 , GRCh37.p13 chr3: 93,779,825-93,780,320 DHFR2, NSUN3
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6311807copy number variation1nstd102humanPathogenic GRCh37 chr3: 93,593,089-93,845,334 , GRCh38.p12 chr3: 93,874,245-94,126,490 PROS1, NSUN3, 7 more genes
    nsv6290878copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,777,422-96,898,993 , GRCh38.p12 chr3: 94,058,578-97,180,149 HNRNPKP4, ARMC10P1, 17 more genes
    nsv4914508copy number variation1nstd200human GRCh38 chr3: 94,062,846-94,063,013 , GRCh37.p13 chr3: 93,781,690-93,781,857 DHFR2, NSUN3
    nsv4914506copy number variation1nstd200human GRCh38 chr3: 93,991,806-94,228,578 , GRCh37.p13 chr3: 93,710,650-93,947,422 DHFR2, RBBP4P2, 3 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4704840copy number variation1nstd195human GRCh37 chr3: 93,674,351-93,791,651 , GRCh38.p12 chr3: 93,955,507-94,072,807 PROS1, NSUN3, 5 more genes
    nsv4701731copy number variation1nstd195human GRCh37 chr3: 93,674,651-93,954,451 , GRCh38.p12 chr3: 93,955,807-94,235,607 PROS1, NSUN3, 6 more genes
    nsv4682065copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,754,175-93,780,355 , GRCh38.p12 chr3: 94,035,331-94,061,511 ARL13B, DHFR2, 1 more genes
    nsv4681867copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,692,518-93,845,334 , GRCh38.p12 chr3: 93,973,674-94,126,490 RNU6-511P, NSUN3, 6 more genes
    nsv4679686copy number variation1nstd189human GRCh37.p13 chr3: 93,519,479-97,386,798 , GRCh38.p12 chr3: 93,800,635-97,667,954 PROS1, NSUN3, 25 more genes
    nsv4679489copy number variation1nstd189human GRCh37.p13 chr3: 93,519,479-94,026,868 , GRCh38.p12 chr3: 93,800,635-94,308,024 PROS1, NSUN3, 8 more genes
    nsv4674369copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 93,516,594-96,012,342 , GRCh38.p12 chr3: 93,797,750-96,293,498 PROS1, NSUN3, 14 more genes
    nsv4596696copy number variation1nstd183human GRCh37 chr3: 93,773,771-93,776,605 , GRCh38.p12 chr3: 94,054,927-94,057,761 ARL13B, DHFR2
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