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Items: 1 to 20 of 105

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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
    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
    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
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4728221copy number variation1nstd102humanUncertain significance GRCh37 chr3: 70,938,608-74,660,846 , GRCh38.p12 chr3: 70,889,457-74,611,695 CCDC137P1, LINC02047, 45 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4374511copy number variation1nstd173human GRCh37 chr3: 72,033,169-72,093,497 , GRCh38.p12 chr3: 71,984,018-72,044,346 UBE2Q2P9, LINC00877, 1 more genes
    nsv3922768copy number variation1nstd102humanPathogenic GRCh37 chr3: 64,746,924-78,459,248 , GRCh38 chr3: 64,761,248-78,410,098 , NCBI36 chr3: 64,721,964-78,541,938 RNU6-557P, LOC105377160, 147 more genes
    nsv3920193copy number variation1nstd102humanPathogenic GRCh37 chr3: 67,441,430-73,463,152 , NCBI36 chr3: 67,524,120-73,545,842 , GRCh38 chr3: 67,391,006-73,414,001 RNPC3P1, LOC105377162, 65 more genes
    nsv3917061copy number variation1nstd102humanPathogenic NCBI36 chr3: 68,940,430-75,092,800 , GRCh37.p13 chr3: 68,857,740-75,010,110 , GRCh38.p12 chr3: 68,808,589-74,960,959 RYBP, GXYLT2, 69 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 more genes
    nsv3913280copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 68,460,820-76,896,160 , GRCh37 chr3: 68,378,130-76,813,470 , GRCh38 chr3: 68,328,980-76,764,319 AKR1B1P2, GPR27, 105 more genes
    nsv3912160copy number variation1nstd102humanPathogenic GRCh38 chr3: 71,317,346-74,324,671 , GRCh37 chr3: 71,366,497-74,373,822 , NCBI36 chr3: 71,449,187-74,456,512 GPR27, LOC105377161, 44 more genes
    nsv3911926copy number variation1nstd102humanPathogenic NCBI36 chr3: 70,428,008-74,996,919 , GRCh38 chr3: 70,296,167-74,865,078 , GRCh37 chr3: 70,345,318-74,914,229 GXYLT2, PDZRN3-AS1, 52 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
    nsv3886687copy number variation1nstd102humanBenign GRCh37 chr3: 72,041,932-72,248,600 , GRCh38.p12 chr3: 71,992,781-72,199,449 LINC00870, UBE2Q2P9, 3 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
    nsv3883532copy number variation1nstd102humanPathogenic GRCh37 chr3: 66,133,719-75,076,440 , GRCh38.p12 chr3: 66,148,044-75,027,289 PSMD12P1, RNU2-64P, 93 more genes
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