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Items: 1 to 20 of 236

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7077376inversion1nstd229human GRCh38 chr12: 16,364,876-16,400,940 , GRCh37.p13 chr12: 16,517,810-16,553,874 SUPT16HP1, MGST1
    nsv7073049inversion1nstd229human GRCh38 chr12: 16,368,997-16,416,184 , GRCh37.p13 chr12: 16,521,931-16,569,118 MGST1, SUPT16HP1
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv6937936copy number variation1nstd229human GRCh38 chr12: 16,352,501-16,398,100 , GRCh37.p13 chr12: 16,505,435-16,551,034 SUPT16HP1, MGST1
    nsv6936477copy number variation1nstd229human GRCh38 chr12: 16,185,413-17,407,405 , GRCh37.p13 chr12: 16,338,347-17,560,339 RPL7P40, LOC105369677, 11 more genes
    nsv6935400copy number variation1nstd229human GRCh38 chr12: 16,347,170-16,354,918 , GRCh37.p13 chr12: 16,500,104-16,507,852 MGST1
    nsv6933613copy number variation1nstd229human GRCh38 chr12: 16,353,287-16,420,147 , GRCh37.p13 chr12: 16,506,221-16,573,081 SUPT16HP1, MGST1
    nsv6933326copy number variation1nstd229human GRCh38 chr12: 16,342,010-16,424,545 , GRCh37.p13 chr12: 16,494,944-16,577,479 MGST1, SUPT16HP1
    nsv6929137copy number variation1nstd229human GRCh38 chr12: 16,376,514-16,376,643 , GRCh37.p13 chr12: 16,529,448-16,529,577 MGST1
    nsv6928354copy number variation1nstd229human GRCh38 chr12: 16,366,469-16,389,287 , GRCh37.p13 chr12: 16,519,403-16,542,221 MGST1
    nsv6925124copy number variation1nstd229human GRCh38 chr12: 15,908,192-16,359,645 , GRCh37.p13 chr12: 16,061,126-16,512,579 LOC101928362, MGST1, 3 more genes
    nsv6924892copy number variation1nstd229human GRCh38 chr12: 16,328,101-16,516,600 , GRCh37.p13 chr12: 16,481,035-16,669,534 GOT2P4, MGST1, 1 more genes
    nsv6922824copy number variation1nstd229human GRCh38 chr12: 16,311,301-16,436,900 , GRCh37.p13 chr12: 16,464,235-16,589,834 SUPT16HP1, MGST1
    nsv6921717copy number variation1nstd229human GRCh38 chr12: 16,281,725-16,498,640 , GRCh37.p13 chr12: 16,434,659-16,651,574 SUPT16HP1, MGST1
    nsv6920936copy number variation1nstd229human GRCh38 chr12: 16,263,257-16,578,862 , GRCh37.p13 chr12: 16,416,191-16,731,796 LMO3, LOC101928362, 4 more genes
    nsv6919401copy number variation1nstd229human GRCh38 chr12: 16,309,174-16,453,535 , GRCh37.p13 chr12: 16,462,108-16,606,469 MGST1, SUPT16HP1
    nsv6918980copy number variation1nstd229human GRCh38 chr12: 16,356,377-16,364,155 , GRCh37.p13 chr12: 16,509,311-16,517,089 MGST1
    nsv6918502copy number variation1nstd229human GRCh38 chr12: 16,314,501-16,396,500 , GRCh37.p13 chr12: 16,467,435-16,549,434 MGST1
    nsv6637209copy number variation1nstd102humanUncertain significance GRCh37 chr12: 16,456,165-16,973,987 , GRCh38.p12 chr12: 16,303,231-16,821,053 LMO3, MGST1, 3 more genes
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