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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
    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
    esv3817972copy number variation24estd214human GRCh37 chrY: 24,390,533-24,409,424 , GRCh38.p12 chrY: 22,244,386-22,263,277 0
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817195copy number variation1683estd214human GRCh37 chrX: 910,112-910,847 , GRCh38.p12 chrX: 949,377-950,112 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
    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
    esv3817752copy number variation714estd214human GRCh37 chrX: 53,819,537-53,820,304 , GRCh38.p12 chrX: 53,793,039-53,793,806
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3817182mobile element insertion208estd214human GRCh37 chrX: 22,365,083-22,365,083 , GRCh38.p12 chrX: 22,346,966-22,346,966 PTCHD1-AS
    esv3817661copy number variation1165estd214human GRCh37 chrX: 154,778,170-154,778,667 , GRCh38.p12 chrX: 155,548,509-155,549,006 TMLHE
    esv3816943mobile element insertion984estd214human GRCh37 chrX: 55,585,160-55,585,160 , GRCh38.p12 chrX: 55,558,727-55,558,727 0
    esv3817570copy number variation815estd214human GRCh37 chrX: 47,352,939-47,353,908 , GRCh38.p12 chrX: 47,493,540-47,494,509 0
    esv3817158copy number variation1708estd214human GRCh37 chrX: 69,302,587-69,303,799 , GRCh38.p12 chrX: 70,082,737-70,083,949 0
    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
    esv3816932copy number variation666estd214human GRCh37 chrX: 41,101,095-41,102,274 , GRCh38.p12 chrX: 41,241,842-41,243,021 0
    esv3817327copy number variation2251estd214human GRCh37 chrX: 144,422,074-144,424,508 , GRCh38.p12 chrX: 145,340,556-145,342,990 0
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