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Items: 1 to 20 of 1153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2678472copy number variation114estd199human GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461 LINC02315
    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
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2665251copy number variation49estd199human GRCh37 chr9: 40,135,245-40,158,892 , GRCh38.p12 chr9: 67,396,719-67,420,087 LOC101927602
    esv2665317copy number variation65estd199human GRCh37 chr11: 7,811,173-7,833,378 , GRCh38.p12 chr11: 7,789,626-7,811,831 , GRCh38.p12 chr11|NT_187583.1: 10,494-32,699 , GRCh38.p12 chr11|NW_011332695.1: 10,494-32,701 OR5P2
    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
    esv2659281copy number variation1estd199human GRCh37 chr2: 53,429,375-53,444,321 , GRCh38.p12 chr2: 53,202,237-53,217,183 LOC105369165
    esv2676497copy number variation51estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2667088copy number variation20estd199human GRCh37 chr4: 98,172,511-98,187,404 , GRCh38.p12 chr4: 97,251,360-97,266,253 STPG2
    esv2657156copy number variation50estd199human GRCh37 chr21: 23,652,945-23,666,892 , GRCh38.p12 chr21: 22,280,625-22,294,572 , GRCh38.p12 chr21|NW_003315968.2: 184,854-198,801 LOC107985508
    esv2678954copy number variation43estd199human GRCh37 chr3: 56,607,727-56,621,584 , GRCh38.p12 chr3: 56,573,699-56,587,556 CCDC66
    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
    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
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