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Items: 1 to 20 of 1348

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2665861copy number variation1estd199human GRCh37 chr2: 67,271,244-67,331,329 , GRCh38.p12 chr2: 67,044,112-67,104,197 LINC01828
    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
    esv2676662copy number variation263estd199human GRCh37 chr19: 41,360,712-41,392,496 , GRCh38.p12 chr19: 40,854,807-40,886,591 CYP2A7
    esv2676981copy number variation78estd199human GRCh37 chr19: 41,345,203-41,375,827 , GRCh38.p12 chr19: 40,839,298-40,869,922 CYP2A6
    esv2662252copy number variation41estd199human GRCh37 chr16: 55,796,145-55,822,792 , GRCh38.p12 chr16: 55,762,233-55,788,880 CES1P1
    esv2678755copy number variation3estd199human GRCh37 chrX: 53,782,064-53,808,307 , GRCh38.p12 chrX: 53,755,566-53,781,809
    esv2664143copy number variation14estd199human GRCh37 chr10: 57,169,095-57,183,342 , GRCh38.p12 chr10: 55,409,335-55,423,582 PCDH15
    esv2663811copy number variation483estd199human GRCh37 chr7: 133,785,000-133,798,329 , GRCh38.p12 chr7: 134,100,247-134,113,576
    esv2669307copy number variation18estd199human GRCh37 chr6: 80,557,132-80,570,423 , GRCh38.p12 chr6: 79,847,415-79,860,706 LOC100422671
    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
    esv2663832copy number variation109estd199human GRCh37 chr4: 118,579,966-118,591,119 , GRCh38.p12 chr4: 117,658,811-117,669,964 LINC01378
    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
    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
    esv2671300copy number variation70estd199human GRCh37 chr12: 133,516,545-133,527,192 , GRCh38.p12 chr12: 132,939,959-132,950,606 ZNF605
    esv2676438copy number variation12estd199human GRCh37 chr2: 233,214,177-233,224,382 , GRCh38.p12 chr2: 232,349,467-232,359,672 ECEL1P3
    esv2661429copy number variation1estd199human GRCh37 chr12: 40,446,319-40,456,481 , GRCh38.p12 chr12: 40,052,517-40,062,679 SLC2A13
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