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Items: 1 to 20 of 174

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5507105copy number variation1nstd206human GRCh38 chr10: 110,587,025-110,588,982 , GRCh37.p13 chr10: 112,346,783-112,348,740 SMC3
    nsv5363352translocation1nstd200human GRCh38 chr6: 122,850,276-122,850,276 , GRCh38 chr10: 110,578,498-110,578,498 , GRCh37.p13 chr10: 112,338,256-112,338,256 , GRCh37.p13 chr6: 123,171,421-123,171,421 SMC3
    nsv5354448translocation1nstd200human GRCh38 chr10: 110,568,709-110,568,709 , GRCh38 chr10: 110,568,626-110,568,626 , GRCh37.p13 chr10: 112,328,384-112,328,384 , GRCh37.p13 chr10: 112,328,467-112,328,467 SMC3
    nsv5304972copy number variation1nstd204human GRCh38.p13 chr10: 110,586,995-110,589,006 , GRCh37.p13 chr10: 112,346,753-112,348,764 SMC3
    nsv5248992copy number variation1nstd204human GRCh38.p13 chr10: 110,586,978-110,588,977 , GRCh37.p13 chr10: 112,346,736-112,348,735 SMC3
    nsv5247075copy number variation1nstd204human GRCh38.p13 chr10: 110,587,001-110,589,000 , GRCh37.p13 chr10: 112,346,759-112,348,758 SMC3
    nsv5208586mobile element deletion1nstd204human GRCh38.p13 chr10: 110,581,212-110,581,525 , GRCh37.p13 chr10: 112,340,970-112,341,283 SMC3
    nsv4970640copy number variation1nstd200human GRCh38 chr10: 110,605,626-110,606,729 , GRCh37.p13 chr10: 112,365,384-112,366,487 SMC3
    nsv4970639copy number variation1nstd200human GRCh38 chr10: 110,587,025-110,588,982 , GRCh37.p13 chr10: 112,346,783-112,348,740 SMC3
    nsv4841649copy number variation1nstd200human GRCh37 chr10: 112,354,307-112,354,399 , GRCh38.p12 chr10: 110,594,549-110,594,641 SMC3
    nsv4839707copy number variation1nstd200human GRCh37 chr10: 112,346,783-112,348,740 , GRCh38.p12 chr10: 110,587,025-110,588,982 SMC3
    nsv4774836mobile element deletion1nstd200human GRCh37 chr10: 112,340,979-112,341,275 , GRCh38.p12 chr10: 110,581,221-110,581,517 SMC3
    nsv4602780copy number variation1nstd183human GRCh37 chr10: 112,281,683-112,358,764 , GRCh38.p12 chr10: 110,521,925-110,599,006 LOC105378483, RPL7P35, 1 more genes
    nsv4348764copy number variation1nstd102humanPathogenic GRCh37 chr10: 110,022,170-135,439,095 , GRCh38.p12 chr10: 108,262,412-133,625,591 LOC105378492, VENTX, 373 more genes
    nsv4339713sequence alteration1nstd166human GRCh37.p13 chr10: 8,718,069-114,609,729 , GRCh38.p12 chr10: 8,676,106-112,849,970 , ADRA2A, 1651 more genes
    nsv4191199copy number variation1nstd166human GRCh37.p13 chr10: 112,338,148-112,338,206 , GRCh38.p12 chr10: 110,578,390-110,578,448 SMC3
    nsv3968774copy number variation1nstd168human GRCh38 chr10: 110,520,033-110,588,615 , GRCh37.p13 chr10: 112,279,791-112,348,373 RPL7P35, LOC105378483, 1 more genes
    nsv3923769copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,194,215-132,432,797 , GRCh37 chr10: 101,953,972-134,246,301 , NCBI36 chr10: 101,943,962-134,096,291 LOC105378493, LINC02627, 477 more genes
    nsv3922274copy number variation1nstd102humanUncertain significance NCBI36 chr10: 103,274,160-135,374,737 , GRCh37.p13 chr10: 103,284,170-135,524,747 , GRCh38.p12 chr10: 101,524,413-133,787,422 DPCD, LOC105378467, 504 more genes
    nsv3921919copy number variation1nstd102humanPathogenic GRCh38 chr10: 100,600,492-133,622,588 , GRCh37 chr10: 102,360,249-135,436,092 , NCBI36 chr10: 102,350,239-135,286,082 MIR4295, BORCS7, 508 more genes
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