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Items: 1 to 20 of 998

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3817210copy number variation589estd214human GRCh37 chrX: 61,950,926-61,955,115 , GRCh38.p12 chrX: 62,731,456-62,735,645 0
    esv3817816copy number variation763estd214human GRCh37 chrX: 131,913,437-131,914,617 , GRCh38.p12 chrX: 132,779,409-132,780,589 HS6ST2
    esv3817218delins1586estd214human GRCh37 chrX: 1,018,298-1,018,298 , GRCh38.p12 chrX: 1,057,563-1,057,563 0
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817660copy number variation618estd214human GRCh37 chrX: 45,423,235-45,423,983 , GRCh38.p12 chrX: 45,563,990-45,564,738 0
    esv3817195copy number variation1683estd214human GRCh37 chrX: 910,112-910,847 , GRCh38.p12 chrX: 949,377-950,112 0
    esv3817679copy number variation1848estd214human GRCh37 chrX: 147,509,695-147,511,237 , GRCh38.p12 chrX: 148,428,176-148,429,718 0
    esv3817610mobile element insertion1552estd214human GRCh37 chrX: 126,290,693-126,290,693 , GRCh38.p12 chrX: 127,156,710-127,156,710 0
    esv3817633copy number variation942estd214human GRCh37 chrX: 153,733,758-153,734,289 , GRCh38.p12 chrX: 154,505,427-154,505,958 FAM3A
    esv3817413delins1094estd214human GRCh37 chrX: 319,122-319,122 , GRCh38.p12 chrX: 358,387-358,387 , GRCh38.p12 chrX|NT_187667.1: 30,880-30,880 , GRCh38.p12 chrX|NT_187634.1: 41,740-41,740 PPP2R3B
    esv3817759copy number variation345estd214human GRCh37 chrX: 27,818,923-27,820,543 , GRCh38.p12 chrX: 27,800,806-27,802,426 0
    esv3817825copy number variation514estd214human GRCh37 chrX: 110,094,444-110,095,367 , GRCh38.p12 chrX: 110,851,216-110,852,139 0
    esv3817191copy number variation775estd214human GRCh37 chrX: 153,634,830-153,636,529 , GRCh38.p12 chrX: 154,406,489-154,408,193 DNASE1L1
    esv3817070copy number variation1108estd214human GRCh37 chrX: 22,377,617-22,378,107 , GRCh38.p12 chrX: 22,359,500-22,359,990 PTCHD1-AS
    esv3817830copy number variation962estd214human GRCh37 chrX: 33,712,708-33,713,545 , GRCh38.p12 chrX: 33,694,591-33,695,428 0
    esv3817167copy number variation489estd214human GRCh37 chrX: 112,443,455-112,444,868 , GRCh38.p12 chrX: 113,200,228-113,201,641 LOC101928437
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3817466copy number variation745estd214human GRCh37 chrX: 105,938,828-105,939,512 , GRCh38.p12 chrX: 106,695,598-106,696,282 RNF128
    esv3817025copy number variation869estd214human GRCh37 chrX: 105,581,825-105,582,814 , GRCh38.p12 chrX: 106,338,596-106,339,585 0
    esv3817485copy number variation757estd214human GRCh37 chrX: 35,323,235-35,324,494 , GRCh38.p12 chrX: 35,305,118-35,306,377 0
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