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Items: 1 to 20 of 1523

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2656818copy number variation1estd199human GRCh37 chr3: 24,745,422-24,820,471 , GRCh38.p12 chr3: 24,703,931-24,778,980 LOC107986070
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2673583copy number variation519estd199human GRCh37 chr20: 1,560,991-1,594,041 , GRCh38.p12 chr20: 1,580,345-1,613,395 SIRPB1
    esv2661656copy number variation43estd199human GRCh37 chr16: 55,794,745-55,823,292 , GRCh38.p12 chr16: 55,760,833-55,789,380 CES1P1
    esv2665251copy number variation49estd199human GRCh37 chr9: 40,135,245-40,158,892 , GRCh38.p12 chr9: 67,396,719-67,420,087 LOC101927602
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2673711copy number variation8estd199human GRCh37 chr16: 74,417,403-74,434,813 , GRCh38.p12 chr16: 74,383,505-74,400,915 NPIPB15
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2677210copy number variation52estd199human GRCh37 chr17: 15,043,901-15,058,721 , GRCh38.p12 chr17: 15,140,584-15,155,404 LOC107984976
    esv2670238copy number variation94estd199human GRCh37 chr17: 15,043,901-15,058,720 , GRCh38.p12 chr17: 15,140,584-15,155,403 LOC107984976
    esv2667151copy number variation1estd199human GRCh37 chr2: 219,275,124-219,289,597 , GRCh38.p12 chr2: 218,410,401-218,424,874 VIL1
    esv2677364copy number variation34estd199human GRCh37 chr7: 91,029,645-91,042,742 , GRCh38.p12 chr7: 91,400,330-91,413,427 LINC02932
    esv2670787copy number variation158estd199human GRCh37 chr7: 151,134-160,557 , GRCh38.p12 chr7: 151,134-160,557 , GRCh38.p12 chr7|NT_187558.1: 106,939-119,904 , GRCh38.p12 chr7|NT_187653.1: 143,455-152,878 LINC03014
    esv2659442copy number variation87estd199human GRCh37 chr7: 150,945-159,992 , GRCh38.p12 chr7: 150,945-159,992 , GRCh38.p12 chr7|NT_187558.1: 106,750-119,335 , GRCh38.p12 chr7|NT_187653.1: 143,266-152,313 LINC03014
    esv2675866copy number variation315estd199human GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813 LOC107987114
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2665944copy number variation17estd199human GRCh37 chr18: 14,449,245-14,461,392 , GRCh38.p12 chr18: 14,449,246-14,461,393 LONRF2P1
    esv2659639copy number variation40estd199human GRCh37 chr15: 76,883,945-76,895,542 , GRCh38.p12 chr15: 76,591,604-76,603,201 SCAPER
    esv2665606copy number variation90estd199human GRCh37 chr7: 91,031,083-91,042,584 , GRCh38.p12 chr7: 91,401,768-91,413,269 LINC02932
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
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