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Items: 1 to 20 of 124

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560640sequence alteration1nstd206human GRCh38 chr3: 140,294,558-140,747,260 , GRCh37.p13 chr3: 140,013,400-140,466,102 CLSTN2, TRIM42, 3 more genes
    nsv5450819copy number variation1nstd206human GRCh38 chr3: 140,211,319-140,831,414 , GRCh37.p13 chr3: 139,930,161-140,550,256 CLSTN2-AS1, LOC102724068, 3 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4728141copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,737,687-142,053,396 , GRCh38.p12 chr3: 139,018,845-142,334,554 RNU6-425P, YWHAQP6, 41 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4451778copy number variation1nstd102humanUncertain significance GRCh37 chr3: 135,186,881-140,826,836 , GRCh38.p12 chr3: 135,468,039-141,107,994 ARMC8, EEF1A1P25, 73 more genes
    nsv4347615copy number variation1nstd102humanPathogenic GRCh37 chr3: 135,288,025-146,874,012 , GRCh38.p12 chr3: 135,569,183-147,156,225 RPL6P9, NME9, 145 more genes
    nsv4343182sequence alteration1nstd166human GRCh37.p13 chr3: 140,013,400-140,466,102 , GRCh38.p12 chr3: 140,294,558-140,747,260 CLSTN2, TRIM42, 3 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv4096663copy number variation1nstd166human GRCh37.p13 chr3: 140,226,651-140,227,092 , GRCh38.p12 chr3: 140,507,809-140,508,250 CLSTN2-AS1, CLSTN2
    nsv3961149inversion1nstd168human GRCh37.p13 chr3: 140,015,906-140,323,756 , GRCh38 chr3: 140,297,064-140,604,914 CLSTN2, CLSTN2-AS1, 2 more genes
    nsv3923685copy number variation1nstd102humanPathogenic GRCh37 chr3: 137,650,842-144,187,581 , NCBI36 chr3: 139,133,532-145,670,271 , GRCh38 chr3: 137,932,000-144,468,739 ATP1B3, RPL23AP40, 97 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
    nsv3921636copy number variation1nstd102humanPathogenic GRCh38 chr3: 135,227,451-145,870,770 , NCBI36 chr3: 136,428,983-147,071,247 , GRCh37 chr3: 134,946,293-145,588,557 A4GNT, TRIM42, 134 more genes
    nsv3921297copy number variation1nstd102humanPathogenic NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585 BFSP2, YWHAQP6, 169 more genes
    nsv3920834copy number variation1nstd102humanUncertain significance NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931 NCK1-DT, LOC107986126, 271 more genes
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