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Items: 1 to 20 of 1138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2667872copy number variation147estd199human GRCh37 chr1: 225,133,630-225,248,654 , GRCh38.p12 chr1: 224,945,928-225,060,952 DNAH14
    esv2665733copy number variation42estd199human GRCh37 chr9: 65,607,845-65,687,792 , GRCh38.p12 chr9: 67,268,943-67,319,293 CNTNAP3P2
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2666578copy number variation167estd199human GRCh37 chr17: 77,462,245-77,494,392 , GRCh38.p12 chr17: 79,466,163-79,498,310 RBFOX3
    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
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    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
    esv2664241copy number variation132estd199human GRCh37 chr21: 23,654,900-23,666,012 , GRCh38.p12 chr21: 22,282,580-22,293,692 , GRCh38.p12 chr21|NW_003315968.2: 186,809-197,921 LOC107985508
    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
    esv2659953copy number variation8estd199human GRCh37 chr5: 41,585,698-41,596,425 , GRCh38.p12 chr5: 41,585,596-41,596,323 TCP1P2
    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
    esv2662536copy number variation311estd199human GRCh37 chr6: 72,863,851-72,873,540 , GRCh38.p12 chr6: 72,154,148-72,163,837 RIMS1
    esv2669406copy number variation54estd199human GRCh37 chr13: 32,530,345-32,539,692 , GRCh38.p12 chr13: 31,956,208-31,965,555 EEF1DP3
    esv2665812copy number variation65estd199human GRCh37 chr15: 31,912,498-31,921,824 , GRCh38.p12 chr15: 31,620,295-31,629,621 , GRCh38.p12 chr15|NT_187660.1: 3,905,446-3,914,773 , GRCh38.p12 chr15|NW_011332701.1: 3,792,994-3,802,321 OTUD7A
    esv2667926copy number variation61estd199human GRCh37 chr11: 107,235,245-107,244,442 , GRCh38.p12 chr11: 107,364,519-107,373,716 CWF19L2
    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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