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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
    esv2666739copy number variation325estd199human GRCh37 chr1: 207,699,545-207,737,892 , GRCh38.p12 chr1: 207,526,200-207,564,547 CR1
    esv2668226copy number variation311estd199human GRCh37 chr3: 129,763,245-129,799,692 , GRCh38.p12 chr3: 130,044,402-130,080,849 ALG1L2
    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
    esv2672539copy number variation26estd199human GRCh37 chrX: 102,778,956-102,809,126 , GRCh38.p12 chrX: 103,524,028-103,554,198 LINC02589
    esv2669475copy number variation624estd199human GRCh37 chr1: 147,976,045-147,996,192 , GRCh38.p12 chr1: 120,848,940-120,869,086 RNVU1-19
    esv2667383copy number variation138estd199human GRCh37 chr2: 98,139,645-98,158,592 , GRCh38.p12 chr2: 97,523,182-97,542,129 ANKRD36B
    esv2669960copy number variation208estd199human GRCh37 chr9: 41,968,745-41,984,492 , GRCh38.p12 chr9: 39,823,727-39,839,474 FGF7P3
    esv2656701copy number variation437estd199human GRCh37 chr16: 78,371,638-78,384,898 , GRCh38.p12 chr16: 78,337,741-78,351,001 WWOX
    esv2672188copy number variation38estd199human GRCh37 chr13: 64,224,636-64,237,600 , GRCh38.p12 chr13: 63,650,503-63,663,467 LOC105370236
    esv2664803copy number variation436estd199human GRCh37 chr15: 76,884,596-76,896,938 , GRCh38.p12 chr15: 76,592,255-76,604,597 SCAPER
    esv2678677copy number variation179estd199human GRCh37 chr15: 76,884,295-76,895,742 , GRCh38.p12 chr15: 76,591,954-76,603,401 SCAPER
    esv2674298copy number variation219estd199human GRCh37 chr1: 35,101,421-35,111,976 , GRCh38.p12 chr1: 34,635,820-34,646,375 LOC105378641
    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
    esv2673043copy number variation328estd199human GRCh37 chr14: 80,106,288-80,115,049 , GRCh38.p12 chr14: 79,639,945-79,648,706 NRXN3
    esv2676043copy number variation92estd199human GRCh37 chr3: 37,978,417-37,986,927 , GRCh38.p12 chr3: 37,936,926-37,945,436 CTDSPL
    esv2677597copy number variation57estd199human GRCh37 chr15: 100,414,545-100,422,992 , GRCh38.p12 chr15: 99,874,340-99,882,787 LOC400464
    esv2678804copy number variation26estd199human GRCh37 chr12: 99,793,445-99,801,692 , GRCh38.p12 chr12: 99,399,667-99,407,914 ANKS1B
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