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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
    esv3817712copy number variation132estd214human GRCh37 chrX: 57,042,827-57,045,791 , GRCh38.p12 chrX: 57,016,394-57,019,358 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
    esv3817887mobile element insertion275estd214human GRCh37 chrX: 95,537,355-95,537,355 , GRCh38.p12 chrX: 96,282,356-96,282,356 0
    esv3817633copy number variation942estd214human GRCh37 chrX: 153,733,758-153,734,289 , GRCh38.p12 chrX: 154,505,427-154,505,958 FAM3A
    esv3817420copy number variation904estd214human GRCh37 chrX: 115,137,622-115,153,304 , GRCh38.p12 chr: NaN-NaN 0
    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
    esv3817154copy number variation887estd214human GRCh37 chrX: 32,886,342-32,886,931 , GRCh38.p12 chrX: 32,868,225-32,868,814 DMD
    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
    esv3817705copy number variation156estd214human GRCh37 chrX: 124,175,457-124,177,951 , GRCh38.p12 chrX: 125,041,608-125,044,102 TENM1
    esv3817191copy number variation775estd214human GRCh37 chrX: 153,634,830-153,636,529 , GRCh38.p12 chrX: 154,406,489-154,408,193 DNASE1L1
    esv3817240copy number variation76estd214human GRCh37 chrX: 41,159,850-41,162,379 , GRCh38.p12 chrX: 41,300,597-41,303,126
    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
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