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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094124copy number variation2nstd102humanUncertain significance GRCh37 chr12: 111,348,881-111,358,333 , GRCh38.p12 chr12: 110,911,077-110,920,529 MYL2
    nsv7094026copy number variation1nstd102humanUncertain significance GRCh37 chr12: 111,356,888-111,358,333 , GRCh38.p12 chr12: 110,919,084-110,920,529 MYL2
    nsv7093956copy number variation1nstd102humanUncertain significance GRCh37 chr12: 111,350,880-111,352,114 , GRCh38.p12 chr12: 110,913,076-110,914,310 MYL2
    nsv7076234inversion1nstd229human GRCh38 chr12: 110,868,174-112,310,507 , GRCh37.p13 chr12: 111,305,978-112,748,311 LOC105369983, RN7SKP71, 35 more genes
    nsv7075330inversion1nstd229human GRCh38 chr12: 110,682,089-111,481,134 , GRCh37.p13 chr12: 111,119,894-111,918,938 LOC105369981, LINC01405, 15 more genes
    nsv7061496inversion1nstd229human GRCh38 chr12: 110,868,674-111,441,001 , GRCh37.p13 chr12: 111,306,478-111,878,805 LOC105369981, LINC01405, 11 more genes
    nsv6932559copy number variation1nstd229human GRCh38 chr12: 110,906,613-110,910,234 , GRCh37.p13 chr12: 111,344,417-111,348,038 CCDC63, MYL2
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6924203copy number variation1nstd229human GRCh38 chr12: 110,912,196-110,914,909 , GRCh37.p13 chr12: 111,350,000-111,352,713 MYL2
    nsv6919347copy number variation1nstd229human GRCh38 chr12: 110,905,765-110,910,176 , GRCh37.p13 chr12: 111,343,569-111,347,980 MYL2, CCDC63
    nsv6918297copy number variation1nstd229human GRCh38 chr12: 110,915,792-110,919,102 , GRCh37.p13 chr12: 111,353,596-111,356,906 MYL2
    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
    nsv6132137copy number variation1nstd213human GRCh37 chr12: 110,580,000-111,480,001 , GRCh38.p12 chr12: 110,142,195-111,042,197 CUX2, IFT81, 21 more genes
    nsv5497361copy number variation1nstd206human GRCh38 chr12: 110,850,066-110,980,043 , GRCh37.p13 chr12: 111,287,870-111,417,847 MYL2, CCDC63, 2 more genes
    nsv5380810copy number variation1nstd102humanUncertain significance GRCh37 chr12: 111,348,861-111,348,999 , GRCh38.p12 chr12: 110,911,057-110,911,195 MYL2
    nsv4995606copy number variation1nstd200human GRCh38 chr12: 110,906,613-110,910,234 , GRCh37.p13 chr12: 111,344,417-111,348,038 CCDC63, MYL2
    nsv4835018copy number variation1nstd200human GRCh37 chr12: 111,344,417-111,348,038 , GRCh38.p12 chr12: 110,906,613-110,910,234 CCDC63, MYL2
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
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