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Items: 1 to 20 of 431

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148271copy number variation1nstd102humanPathogenic GRCh38 chr18: 158,286-14,124,574 , GRCh37.p13 chr18: 158,286-14,124,573 PMM2P2, EIF4A2P1, 225 more genes
    nsv7098917copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-15,400,035 , GRCh38.p12 chr18: 10,001-15,400,036 RNU7-25P, RPL6P27, 275 more genes
    nsv7077580inversion1nstd229human GRCh38 chr18: 2,241,965-2,709,179 , GRCh37.p13 chr18: 2,241,965-2,709,177 SMCHD1, NDC80, 6 more genes
    nsv7077283inversion1nstd229human GRCh38 chr18: 1,541,085-2,638,303 , GRCh37.p13 chr18: 1,541,086-2,638,302 AIDAP3, METTL4, 8 more genes
    nsv7072377inversion1nstd229human GRCh38 chr18: 2,445,680-2,588,176 , GRCh37.p13 chr18: 2,445,679-2,588,175 NDC80, LOC100128926, 1 more genes
    nsv7069073inversion1nstd229human GRCh38 chr18: 1,772,246-2,770,891 , GRCh37.p13 chr18: 1,772,247-2,770,889 AIDAP3, LOC105371957, 11 more genes
    nsv6996060copy number variation1nstd229human GRCh38 chr18: 2,550,620-2,553,962 , GRCh37.p13 chr18: 2,550,619-2,553,961 METTL4
    nsv6994130copy number variation1nstd229human GRCh38 chr18: 2,562,001-2,568,500 , GRCh37.p13 chr18: 2,562,000-2,568,499 LOC100128926, METTL4
    nsv6993959copy number variation1nstd229human GRCh38 chr18: 2,558,656-2,561,631 , GRCh37.p13 chr18: 2,558,655-2,561,630 METTL4
    nsv6992699copy number variation1nstd229human GRCh38 chr18: 2,521,124-2,540,342 , GRCh37.p13 chr18: 2,521,123-2,540,341 METTL4
    nsv6985945copy number variation1nstd229human GRCh38 chr18: 2,541,281-2,583,874 , GRCh37.p13 chr18: 2,541,280-2,583,873 LOC100128926, NDC80, 1 more genes
    nsv6983854copy number variation1nstd229human GRCh38 chr18: 2,263,904-2,568,114 , GRCh37.p13 chr18: 2,263,904-2,568,113 LOC100128926, LOC105371961, 1 more genes
    nsv6983665copy number variation1nstd229human GRCh38 chr18: 2,559,701-2,568,900 , GRCh37.p13 chr18: 2,559,700-2,568,899 METTL4, LOC100128926
    nsv6981987copy number variation1nstd229human GRCh38 chr18: 2,557,601-2,562,900 , GRCh37.p13 chr18: 2,557,600-2,562,899 METTL4
    nsv6979761copy number variation1nstd229human GRCh38 chr18: 2,557,550-2,562,903 , GRCh37.p13 chr18: 2,557,549-2,562,902 METTL4
    nsv6979047copy number variation1nstd229human GRCh38 chr18: 2,083,787-2,663,484 , GRCh37.p13 chr18: 2,083,788-2,663,483 LOC105371961, KATNBL1P3, 7 more genes
    nsv6637695copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,280,228-2,555,929 , GRCh38.p12 chr18: 2,280,229-2,555,930 LOC105371961, METTL4
    nsv6637665copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,255,007-4,488,934 , GRCh38.p12 chr18: 2,255,007-4,488,934 DLGAP1-AS4, MYL12-AS1, 38 more genes
    nsv6637580copy number variation1nstd102humanPathogenic GRCh37 chr18: 136,227-7,218,594 , GRCh38.p12 chr18: 136,227-7,218,596 L3MBTL4-AS1, LOC101927044, 106 more genes
    nsv6637521copy number variation1nstd102humanUncertain significance GRCh37 chr18: 2,485,817-4,086,341 , GRCh38.p12 chr18: 2,485,818-4,086,341 DLGAP1-AS4, EMILIN2, 35 more genes
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