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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    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
    nsv3965694copy number variation1nstd168human GRCh38 chr3: 94,017,767-94,092,004 , GRCh37.p13 chr3: 93,736,611-93,810,848 STX19, NSUN3, 3 more genes
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3920925copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,519,464-94,511,668 , GRCh38 chr3: 93,800,620-94,792,824 , NCBI36 chr3: 95,002,154-95,994,358 RBBP4P2, RNU6-511P, 10 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
    nsv3917160copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903 ATP6V1A, RPS10P4, 297 more genes
    nsv3913190copy number variation1nstd102humanUncertain significance NCBI36 chr3: 95,010,365-95,987,181 , GRCh37 chr3: 93,527,675-94,504,491 , GRCh38 chr3: 93,808,831-94,785,647 NSUN3, PROS1, 10 more genes
    nsv3911724copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 95,021,157-105,090,283 , GRCh37 chr3: 93,538,467-103,607,593 , GRCh38 chr3: 93,819,623-103,888,749 COL8A1, CPOX, 132 more genes
    nsv3911264copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,575,285-94,427,263 , GRCh38 chr3: 93,856,441-94,708,419 , NCBI36 chr3: 95,057,975-95,909,953 HMGN1P7, ARMC10P1, 9 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 2875 more genes
    nsv3872721copy number variation1nstd102humanUncertain significance GRCh37 chr3: 93,519,464-94,500,476 , GRCh38.p12 chr3: 93,800,620-94,781,632 ARL13B, HMGN1P7, 10 more genes
    nsv3136686copy number variation2nstd151human GRCh37 chr3: 93,593,086-93,814,003 , GRCh38.p12 chr3: 93,874,242-94,095,159 RNU6-511P, NSUN3, 7 more genes
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