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Items: 1 to 20 of 297

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6737186copy number variation1nstd229human GRCh38 chr3: 167,864,701-168,010,900 , GRCh37.p13 chr3: 167,582,489-167,728,688 LRRC77P, MEMO1P3, 2 more genes
    nsv6736964copy number variation1nstd229human GRCh38 chr3: 167,985,601-168,010,800 , GRCh37.p13 chr3: 167,703,389-167,728,588 GOLIM4
    nsv6736523copy number variation1nstd229human GRCh38 chr3: 168,081,174-168,081,898 , GRCh37.p13 chr3: 167,798,962-167,799,686 GOLIM4
    nsv6736131copy number variation1nstd229human GRCh38 chr3: 167,912,201-168,011,100 , GRCh37.p13 chr3: 167,629,989-167,728,888 GOLIM4, HMGN2P26, 1 more genes
    nsv6734985copy number variation1nstd229human GRCh38 chr3: 167,983,901-168,011,000 , GRCh37.p13 chr3: 167,701,689-167,728,788 GOLIM4
    nsv6733502copy number variation1nstd229human GRCh38 chr3: 167,988,101-168,011,000 , GRCh37.p13 chr3: 167,705,889-167,728,788 GOLIM4
    nsv6729672copy number variation1nstd229human GRCh38 chr3: 167,947,201-168,011,100 , GRCh37.p13 chr3: 167,664,989-167,728,888 GOLIM4, HMGN2P26
    nsv6729429copy number variation1nstd229human GRCh38 chr3: 167,984,601-168,011,000 , GRCh37.p13 chr3: 167,702,389-167,728,788 GOLIM4
    nsv6729117copy number variation1nstd229human GRCh38 chr3: 167,928,501-168,010,900 , GRCh37.p13 chr3: 167,646,289-167,728,688 HMGN2P26, GOLIM4
    nsv6728337copy number variation1nstd229human GRCh38 chr3: 167,986,801-168,011,200 , GRCh37.p13 chr3: 167,704,589-167,728,988 GOLIM4
    nsv6728310copy number variation1nstd229human GRCh38 chr3: 167,877,101-168,010,400 , GRCh37.p13 chr3: 167,594,889-167,728,188 LRRC77P, HMGN2P26, 2 more genes
    nsv6722462copy number variation1nstd229human GRCh38 chr3: 168,035,601-168,038,200 , GRCh37.p13 chr3: 167,753,389-167,755,988 GOLIM4
    nsv6721684copy number variation1nstd229human GRCh38 chr3: 168,054,104-168,059,550 , GRCh37.p13 chr3: 167,771,892-167,777,338 GOLIM4
    nsv6721676copy number variation1nstd229human GRCh38 chr3: 168,035,801-168,038,300 , GRCh37.p13 chr3: 167,753,589-167,756,088 GOLIM4
    nsv6721524copy number variation1nstd229human GRCh38 chr3: 167,866,301-168,010,600 , GRCh37.p13 chr3: 167,584,089-167,728,388 HMGN2P26, GOLIM4, 2 more genes
    nsv6719642copy number variation1nstd229human GRCh38 chr3: 167,869,201-168,011,000 , GRCh37.p13 chr3: 167,586,989-167,728,788 MEMO1P3, LRRC77P, 2 more genes
    nsv6719497copy number variation1nstd229human GRCh38 chr3: 167,870,301-168,010,700 , GRCh37.p13 chr3: 167,588,089-167,728,488 LRRC77P, MEMO1P3, 2 more genes
    nsv6718677copy number variation1nstd229human GRCh38 chr3: 168,000,380-168,008,479 , GRCh37.p13 chr3: 167,718,168-167,726,267 GOLIM4
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6365171copy number variation1nstd223human GRCh38 chr3: 168,066,286-168,066,786 , GRCh37.p13 chr3: 167,784,074-167,784,574 GOLIM4
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