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Items: 1 to 20 of 1589

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2675987copy number variation1estd199human GRCh37 chr4: 182,628,182-182,644,168 , GRCh38.p12 chr4: 181,707,029-181,723,015 TENM3
    esv2666573copy number variation1estd199human GRCh37 chr4: 182,628,115-182,643,979 , GRCh38.p12 chr4: 181,706,962-181,722,826 TENM3
    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
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    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
    esv2674705copy number variation19estd199human GRCh37 chr5: 17,637,706-17,650,425 , GRCh38.p12 chr5: 17,637,597-17,650,316 LOC391768
    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
    esv2664407copy number variation27estd199human GRCh37 chr5: 17,639,241-17,651,719 , GRCh38.p12 chr5: 17,639,132-17,651,610 LOC391768
    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
    esv2667645copy number variation26estd199human GRCh37 chr8: 2,150,546-2,161,598 , GRCh38.p12 chr8: 2,202,907-2,213,931 , GRCh38.p12 chr8|NT_187576.1: 385,756-396,808 LOC105377782
    esv2674298copy number variation219estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    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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