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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
    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
    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
    esv3817863copy number variation5estd214human GRCh37 chrX: 828,660-829,916 , GRCh38.p12 chrX: 867,925-869,181 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
    esv3817752copy number variation714estd214human GRCh37 chrX: 53,819,537-53,820,304 , GRCh38.p12 chrX: 53,793,039-53,793,806
    esv3817830copy number variation962estd214human GRCh37 chrX: 33,712,708-33,713,545 , GRCh38.p12 chrX: 33,694,591-33,695,428 0
    esv3817383copy number variation159estd214human GRCh37 chrX: 819,642-825,644 , GRCh38.p12 chrX: 858,907-864,909 0
    esv3817869copy number variation10estd214human GRCh37 chrX: 32,929,238-32,969,915 , GRCh38.p12 chrX: 32,911,121-32,951,798 DMD
    esv3816956copy number variation1245estd214human GRCh37 chrX: 97,167,898-97,168,316 , GRCh38.p12 chrX: 97,912,900-97,913,318 0
    esv3817436copy number variation215estd214human GRCh37 chrX: 94,577,293-94,578,659 , GRCh38.p12 chrX: 95,322,294-95,323,660 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
    esv3817694copy number variation502estd214human GRCh37 chrX: 24,184,245-24,185,065 , GRCh38.p12 chrX: 24,166,128-24,166,948 ZFX
    esv3817829copy number variation603estd214human GRCh37 chrX: 48,500,496-48,502,930 , GRCh38.p12 chrX: 48,642,108-48,644,542 0
    esv3817153copy number variation667estd214human GRCh37 chrX: 53,481,170-53,482,871 , GRCh38.p12 chrX: 53,454,223-53,455,924 TIPINP1
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