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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137136copy number variation1nstd102humanUncertain significance GRCh37 chr12: 108,917,234-109,052,695 , GRCh38.p12 chr12: 108,523,457-108,658,919 ISCU, TMEM119, 5 more genes
    nsv7061495inversion1nstd229human GRCh38 chr12: 107,014,490-109,497,170 , GRCh37.p13 chr12: 107,408,268-109,934,975 RPL17P38, RNU6-361P, 46 more genes
    nsv6937560copy number variation1nstd229human GRCh38 chr12: 107,811,784-108,715,214 , GRCh37.p13 chr12: 108,205,561-109,108,990 ISCU, LOC105369964, 16 more genes
    nsv6936377copy number variation1nstd229human GRCh38 chr12: 108,539,333-108,542,325 , GRCh37.p13 chr12: 108,933,109-108,936,101 SART3
    nsv6931539copy number variation1nstd229human GRCh38 chr12: 108,539,272-108,544,506 , GRCh37.p13 chr12: 108,933,048-108,938,282 SART3
    nsv6930841copy number variation1nstd229human GRCh38 chr12: 108,473,032-108,651,457 , GRCh37.p13 chr12: 108,866,809-109,045,233 SELPLG, SART3, 7 more genes
    nsv6922947copy number variation1nstd229human GRCh38 chr12: 108,490,015-109,627,369 , GRCh37.p13 chr12: 108,883,792-110,065,174 RNU4-32P, LOC105369968, 30 more genes
    nsv6592194inversion1nstd223human GRCh38 chr12: 108,541,121-108,541,745 , GRCh37.p13 chr12: 108,934,897-108,935,521 SART3
    nsv6495074copy number variation1nstd223human GRCh38 chr12: 108,551,301-108,553,500 , GRCh37.p13 chr12: 108,945,077-108,947,276 SART3
    nsv6493811copy number variation1nstd223human GRCh38 chr12: 108,539,333-108,542,325 , GRCh37.p13 chr12: 108,933,109-108,936,101 SART3
    nsv6491868copy number variation1nstd223human GRCh38 chr12: 108,551,562-108,552,318 , GRCh37.p13 chr12: 108,945,338-108,946,094 SART3
    nsv6484820copy number variation1nstd223human GRCh38 chr12: 108,533,362-108,566,515 , GRCh37.p13 chr12: 108,927,138-108,960,291 SART3, ISCU
    nsv6470333copy number variation1nstd223human GRCh38 chr12: 107,811,784-108,715,214 , GRCh37.p13 chr12: 108,205,561-109,108,990 LOC105369965, LINC01498, 16 more genes
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132406copy number variation1nstd213human GRCh37 chr12: 108,420,000-110,500,001 , GRCh38.p12 chr12: 108,026,223-110,062,196 DAO, SART3, 47 more genes
    nsv6083247insertion1nstd212human GRCh38 chr12: 108,533,211-108,533,211 , GRCh37.p13 chr12: 108,926,987-108,926,987 SART3
    nsv6039310copy number variation1nstd212human GRCh38 chr12: 108,539,334-108,542,327 , GRCh37.p13 chr12: 108,933,110-108,936,103 SART3
    nsv5934353copy number variation1nstd209human GRCh38 chr12: 108,539,333-108,542,324 , GRCh37.p13 chr12: 108,933,109-108,936,100 SART3
    nsv5864272copy number variation1nstd209human GRCh38 chr12: 108,539,337-108,542,065 , GRCh37.p13 chr12: 108,933,113-108,935,841 SART3
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