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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
    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
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2674647copy number variation204estd199human GRCh37 chr8: 56,377,729-56,393,641 , GRCh38.p12 chr8: 55,465,169-55,481,081 XKR4
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    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
    esv2666505copy number variation53estd199human GRCh37 chr3: 195,457,318-195,471,074 , GRCh38.p12 chr3|NT_187678.1: 51,829-65,597 , GRCh38.p12 chr3|NT_187688.1: 50,529-64,252 , GRCh38.p12 chr3|NT_187689.1: 100,944-114,700 , GRCh38.p12 chr3|NT_187690.1: 50,528-64,259 , GRCh38.p12 chr3|NT_187691.1: 50,635-64,429 , GRCh38.p12 chr3|NT_187532.1: 100,944-114,700 , GRCh38.p12 chr3|NT_187649.1: 50,533-64,252 , GRCh38.p12 chr3: 195,730,447-195,744,203 MUC20
    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
    esv2675519copy number variation112estd199human GRCh37 chr18: 66,745,594-66,756,999 , GRCh38.p12 chr18: 69,078,357-69,089,762 CCDC102B
    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
    esv2673513copy number variation1estd199human GRCh37 chr10: 12,540,425-12,549,931 , GRCh38.p12 chr10: 12,498,426-12,507,932 CAMK1D
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