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Items: 1 to 20 of 1141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2674484copy number variation82estd199human GRCh37 chr1: 225,133,646-225,248,670 , GRCh38.p12 chr1: 224,945,944-225,060,968 DNAH14
    esv2678472copy number variation114estd199human GRCh37 chr14: 41,609,436-41,669,664 , GRCh38.p12 chr14: 41,140,233-41,200,461 LINC02315
    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
    esv2666901copy number variation459estd199human GRCh37 chr11: 1,915,249-1,937,009 , GRCh38.p12 chr11: 1,894,019-1,915,779 LINC01150
    esv2660674copy number variation20estd199human GRCh37 chr18: 14,550,245-14,567,792 , GRCh38.p12 chr18: 14,550,246-14,567,793 LOC105372004
    esv2672929copy number variation23estd199human GRCh37 chr16: 60,081,112-60,098,561 , GRCh38.p12 chr16: 60,047,208-60,064,657 LINC02141
    esv2662901copy number variation324estd199human GRCh37 chr9: 41,969,445-41,984,392 , GRCh38.p12 chr9: 39,824,427-39,839,374 FGF7P3
    esv2664983copy number variation7estd199human GRCh37 chr5: 114,706,251-114,721,123 , GRCh38.p12 chr5: 115,370,554-115,385,426 LOC105379130
    esv2660454copy number variation12estd199human GRCh37 chr6: 31,274,445-31,288,892 , GRCh38.p12 chr6: 31,306,668-31,321,115 LOC112267902
    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
    esv2675866copy number variation315estd199human GRCh37 chr9: 113,024,576-113,037,093 , GRCh38.p12 chr9: 110,262,296-110,274,813 LOC107987114
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2662987copy number variation3estd199human GRCh37 chr21: 17,776,955-17,789,175 , GRCh38.p12 chr21: 16,404,635-16,416,855 MIR99AHG
    esv2662662copy number variation3estd199human GRCh37 chr3: 88,468,041-88,480,082 , GRCh38.p12 chr3: 88,418,891-88,430,932 CSNKA2IP
    esv2658100copy number variation4estd199human GRCh37 chr3: 88,468,183-88,480,125 , GRCh38.p12 chr3: 88,419,033-88,430,975 CSNKA2IP
    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
    esv2677965copy number variation40estd199human GRCh37 chr4: 92,073,713-92,084,451 , GRCh38.p12 chr4: 91,152,562-91,163,300 CCSER1
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