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Items: 1 to 20 of 2732

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4684017copy number variation142nstd187human GRCh37 chr8: 6,872,895-6,876,338 , GRCh38.p12 chr8: 7,015,373-7,018,816 , GRCh38.p12 chr8|NW_018654717.1: 410,494-413,940 DEFA3
    esv3817218delins1586estd214human GRCh37 chrX: 1,018,298-1,018,298 , GRCh38.p12 chrX: 1,057,563-1,057,563 0
    esv3817754mobile element insertion601estd214human GRCh37 chrX: 14,152,015-14,152,015 , GRCh38.p12 chrX: 14,133,896-14,133,896 0
    esv3817535copy number variation3estd214human GRCh37 chrX: 20,138,974-20,138,974 , GRCh38.p12 chrX: 20,120,856-20,120,856 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
    esv3817191copy number variation775estd214human GRCh37 chrX: 153,634,830-153,636,529 , GRCh38.p12 chrX: 154,406,489-154,408,193 DNASE1L1
    esv3816979mobile element insertion201estd214human GRCh37 chrX: 31,470,360-31,470,360 , GRCh38.p12 chrX: 31,452,243-31,452,243 DMD
    esv3817070copy number variation1108estd214human GRCh37 chrX: 22,377,617-22,378,107 , GRCh38.p12 chrX: 22,359,500-22,359,990 PTCHD1-AS
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3816943mobile element insertion984estd214human GRCh37 chrX: 55,585,160-55,585,160 , GRCh38.p12 chrX: 55,558,727-55,558,727 0
    esv3817710copy number variation1286estd214human GRCh37 chrX: 78,921,957-78,926,007 , GRCh38.p12 chrX: 79,666,460-79,670,510 0
    esv3817295mobile element insertion62estd214human GRCh37 chrX: 101,439,260-101,439,260 , GRCh38.p12 chrX: 102,184,287-102,184,287 TCP11X3P
    esv3817393mobile element insertion564estd214human GRCh37 chrX: 121,569,332-121,569,332 , GRCh38.p12 chrX: 122,435,479-122,435,479 LOC101928359
    esv3817274copy number variation1608estd214human GRCh37 chrX: 40,461,270-40,461,776 , GRCh38.p12 chrX: 40,602,018-40,602,524 ATP6AP2
    esv3817522copy number variation1092estd214human GRCh37 chrX: 71,357,127-71,357,564 , GRCh38.p12 chrX: 72,137,277-72,137,714 NHSL2
    esv3816996delins61estd214human GRCh37 chrX: 32,354,004-32,354,004 , GRCh38.p12 chrX: 32,335,887-32,335,887 DMD
    esv3817458copy number variation1061estd214human GRCh37 chrX: 131,744,448-131,745,660 , GRCh38.p12 chrX: 132,610,420-132,611,632 0
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