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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
    esv3817038copy number variation3estd214human GRCh37 chrX: 13,829,184-13,829,184 , GRCh38.p12 chrX: 13,811,065-13,811,065 GPM6B
    esv3817884copy number variation1789estd214human GRCh37 chrX: 131,089,382-131,089,611 , GRCh38.p12 chrX: 131,955,354-131,955,583 0
    esv3817451copy number variation109estd214human GRCh37 chrX: 84,782,034-84,783,795 , GRCh38.p12 chrX: 85,527,029-85,528,790 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
    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
    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
    esv3816989mobile element insertion84estd214human GRCh37 chrX: 138,744,482-138,744,482 , GRCh38.p12 chrX: 139,662,323-139,662,323 MCF2
    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
    esv3817075copy number variation25estd214human GRCh37 chrX: 6,032,449-6,035,568 , GRCh38.p12 chrX: 6,114,408-6,117,527 NLGN4X
    esv3817436copy number variation215estd214human GRCh37 chrX: 94,577,293-94,578,659 , GRCh38.p12 chrX: 95,322,294-95,323,660 0
    esv3817694copy number variation502estd214human GRCh37 chrX: 24,184,245-24,185,065 , GRCh38.p12 chrX: 24,166,128-24,166,948 ZFX
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