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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902904copy number variation1nstd209human GRCh38 chr3: 66,803,410-74,489,186 , GRCh37.p13 chr3: 66,853,834-74,538,337 , LOC105377160, 83 more genes
    nsv5723859mobile element insertion1nstd211human GRCh38 chr3: 70,216,956-70,216,956 , GRCh37.p13 chr3: 70,266,107-70,266,107 MDFIC2
    nsv5686852mobile element insertion2nstd211human GRCh38 chr3: 70,274,408-70,274,408 , GRCh37.p13 chr3: 70,323,559-70,323,559 MDFIC2
    nsv5564784copy number variation1nstd207human GRCh38 chr3: 70,211,308-70,211,366 , GRCh37.p13 chr3: 70,260,459-70,260,517 MDFIC2
    nsv5564432copy number variation1nstd102humanPathogenic GRCh37 chr3: 68,939,251-72,700,418 , GRCh38.p12 chr3: 68,890,100-72,651,267 CCDC137P1, LOC105377160, 39 more genes
    nsv5449074copy number variation1nstd206human GRCh38 chr3: 70,310,930-70,315,335 , GRCh37.p13 chr3: 70,360,081-70,364,486 MDFIC2
    nsv5405089mobile element insertion1nstd206human GRCh38 chr3: 70,274,408-70,274,459 , GRCh37.p13 chr3: 70,323,559-70,323,610 MDFIC2
    nsv5099392mobile element insertion1nstd203human GRCh38 chr3: 70,274,389-70,274,408 , GRCh37.p13 chr3: 70,323,540-70,323,559 MDFIC2
    nsv5098959mobile element insertion1nstd203human GRCh38 chr3: 70,274,394-70,274,408 , GRCh37.p13 chr3: 70,323,545-70,323,559 MDFIC2
    nsv5098785mobile element insertion1nstd203human GRCh38 chr3: 70,274,397-70,274,408 , GRCh37.p13 chr3: 70,323,548-70,323,559 MDFIC2
    nsv5092850mobile element insertion1nstd203human GRCh38 chr3: 70,274,391-70,274,408 , GRCh37.p13 chr3: 70,323,542-70,323,559 MDFIC2
    nsv5091792mobile element insertion1nstd203human GRCh38 chr3: 70,197,431-70,197,447 , GRCh37.p13 chr3: 70,246,582-70,246,598 MDFIC2
    nsv5084646mobile element insertion1nstd203human GRCh38 chr3: 70,274,393-70,274,408 , GRCh37.p13 chr3: 70,323,544-70,323,559 MDFIC2
    nsv5081047mobile element insertion1nstd203human GRCh38 chr3: 70,274,392-70,274,408 , GRCh37.p13 chr3: 70,323,543-70,323,559 MDFIC2
    nsv5033386inversion1nstd200human GRCh38 chr3: 66,830,019-82,426,887 , GRCh37.p13 chr3: 66,880,443-82,476,038 , HNRNPA3P6, 150 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4927302copy number variation1nstd200human GRCh38 chr3: 70,205,917-70,206,104 , GRCh37.p13 chr3: 70,255,068-70,255,255 MDFIC2
    nsv4918794copy number variation1nstd200human GRCh38 chr3: 70,297,057-70,300,166 , GRCh37.p13 chr3: 70,346,208-70,349,317 MDFIC2
    nsv4918793copy number variation1nstd200human GRCh38 chr3: 70,236,506-70,236,623 , GRCh37.p13 chr3: 70,285,657-70,285,774 MDFIC2
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
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