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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    esv2667697copy number variation42estd199human GRCh37 chr7: 141,765,556-141,794,588 , GRCh38.p12 chr7: 142,065,756-142,094,788 , GRCh38.p12 chr7|NT_187562.1: 27,636-56,668 MGAM
    esv2661656copy number variation43estd199human GRCh37 chr16: 55,794,745-55,823,292 , GRCh38.p12 chr16: 55,760,833-55,789,380 CES1P1
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2671576copy number variation156estd199human GRCh37 chr7: 100,326,645-100,341,192 , GRCh38.p12 chr7: 100,729,022-100,743,569 ZAN
    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
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    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
    esv2665944copy number variation17estd199human GRCh37 chr18: 14,449,245-14,461,392 , GRCh38.p12 chr18: 14,449,246-14,461,393 LONRF2P1
    esv2675135copy number variation79estd199human GRCh37 chr3: 53,027,148-53,038,898 , GRCh38.p12 chr3: 52,993,132-53,004,882 SFMBT1
    esv2659375copy number variation188estd199human GRCh37 chr21: 23,654,900-23,666,003 , GRCh38.p12 chr21: 22,282,580-22,293,683 , GRCh38.p12 chr21|NW_003315968.2: 186,809-197,912 LOC107985508
    esv2672284copy number variation80estd199human GRCh37 chr11: 107,233,995-107,244,392 , GRCh38.p12 chr11: 107,363,269-107,373,666 CWF19L2
    esv2673551copy number variation872estd199human GRCh37 chr3: 192,875,329-192,885,405 , GRCh38.p12 chr3: 193,157,540-193,167,616 VEZF1P1
    esv2675979copy number variation520estd199human GRCh37 chr6: 53,924,803-53,934,828 , GRCh38.p12 chr6: 54,060,005-54,070,030 MLIP
    esv2657260copy number variation826estd199human GRCh37 chr2: 87,730,745-87,740,792 , GRCh38.p12 chr2: 87,431,226-87,441,083 LINC01943
    esv2676043copy number variation92estd199human GRCh37 chr3: 37,978,417-37,986,927 , GRCh38.p12 chr3: 37,936,926-37,945,436 CTDSPL
    esv2659844copy number variation372estd199human GRCh37 chr6: 53,925,724-53,934,162 , GRCh38.p12 chr6: 54,060,926-54,069,364 MLIP
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