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Items: 1 to 20 of 245

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968000inversion1nstd209human GRCh38 chr22: 23,676,272-24,601,321 , GRCh37.p13 chr22: 24,018,459-24,997,288 , ADORA2A, 38 more genes
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5540924copy number variation1nstd206human GRCh38 chr22: 23,761,584-23,762,368 , GRCh37.p13 chr22: 24,103,771-24,104,555 C22orf15
    nsv5381153copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,915,453-24,921,762 , GRCh38.p12 chr22: 23,573,266-24,525,794 GSTT2B, SUSD2, 37 more genes
    nsv5381087copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,699,269-24,992,266 , GRCh38.p12 chr22: 23,357,082-24,596,299 LOC100129358, VPREB3, 49 more genes
    nsv5033192copy number variation1nstd200human GRCh38 chr22: 23,765,574-23,767,297 , GRCh37.p13 chr22: 24,107,761-24,109,484 LOC107985577, C22orf15, 1 more genes
    nsv5031862copy number variation1nstd200human GRCh38 chr22: 23,765,605-23,766,344 , GRCh37.p13 chr22: 24,107,792-24,108,531 C22orf15, CHCHD10, 1 more genes
    nsv4869185copy number variation1nstd200human GRCh37 chr22: 24,107,790-24,109,457 , GRCh38.p12 chr22|NT_187633.1: 1,965-3,632 , GRCh38.p12 chr22: 23,765,603-23,767,270 C22orf15, CHCHD10, 1 more genes
    nsv4869184copy number variation1nstd200human GRCh37 chr22: 24,107,792-24,108,531 , GRCh38.p12 chr22: 23,765,605-23,766,344 , GRCh38.p12 chr22|NT_187633.1: 1,967-2,706 LOC107985577, CHCHD10, 1 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4729959copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,650,873-25,043,046 , GRCh38.p12 chr22: 23,308,686-24,647,079 BCRP1, SNRPD3, 55 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729872copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,258,368-25,059,827 , GRCh38.p12 chr22: 22,916,198-24,663,860 LOC105372957, RAB36, 71 more genes
    nsv4729784copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,720,181-25,066,484 , GRCh38.p12 chr22: 23,377,994-24,670,517 POM121L10P, GGTLC4P, 51 more genes
    nsv4681263copy number variation1nstd102humanUncertain significance GRCh37 chr22: 24,108,011-24,109,790 , GRCh38.p12 chr22: 23,765,824-23,767,603 , GRCh38.p12 chr22|NT_187633.1: 2,186-3,965 LOC107985577, CHCHD10, 1 more genes
    nsv4681014copy number variation1nstd189human GRCh37.p13 chr22: 23,685,680-25,034,432 , GRCh38.p12 chr22: 23,343,493-24,638,465 , ADORA2A, 51 more genes
    nsv4681006copy number variation1nstd189human GRCh37.p13 chr22: 23,689,984-25,039,192 , GRCh38.p12 chr22: 23,347,797-24,643,225 , ADORA2A, 52 more genes
    nsv4679621copy number variation1nstd189human GRCh37.p13 chr22: 23,008,722-25,047,777 , GRCh38.p12 chr22: 22,666,252-24,651,810 , ADORA2A, 120 more genes
    nsv4679148copy number variation1nstd189human GRCh37.p13 chr22: 23,635,698-24,582,739 , GRCh38.p12 chr22: 23,293,511-24,186,771 , ASLP1, 39 more genes
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