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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
    nsv5493531copy number variation1nstd206human GRCh38 chr8: 52,552,369-52,957,222 , GRCh37.p13 chr8: 53,464,929-53,869,782 RB1CC1, LOC105375835, 3 more genes
    nsv5487891copy number variation1nstd206human GRCh38 chr8: 52,930,374-53,029,819 , GRCh37.p13 chr8: 53,842,934-53,942,379 LOC101060191, NPBWR1
    nsv5478594copy number variation1nstd206human GRCh38 chr8: 52,940,749-52,961,623 , GRCh37.p13 chr8: 53,853,309-53,874,183 NPBWR1
    nsv5473999copy number variation1nstd206human GRCh38 chr8: 52,827,224-52,953,903 , GRCh37.p13 chr8: 53,739,784-53,866,463 NPBWR1, LOC107986943
    nsv4965318copy number variation1nstd200human GRCh38 chr8: 52,930,374-53,029,819 , GRCh37.p13 chr8: 53,842,934-53,942,379 LOC101060191, NPBWR1
    nsv4965316copy number variation1nstd200human GRCh38 chr8: 52,876,349-53,012,584 , GRCh37.p13 chr8: 53,788,909-53,925,144 LOC101060191, NPBWR1, 1 more genes
    nsv4965314copy number variation1nstd200human GRCh38 chr8: 52,793,242-52,951,645 , GRCh37.p13 chr8: 53,705,802-53,864,205 NPBWR1, LOC107986943
    nsv4965313copy number variation1nstd200human GRCh38 chr8: 52,783,971-52,968,651 , GRCh37.p13 chr8: 53,696,531-53,881,211 LOC107986943, NPBWR1
    nsv4965296copy number variation1nstd200human GRCh38 chr8: 52,459,403-53,003,191 , GRCh37.p13 chr8: 53,371,963-53,915,751 NPBWR1, LOC107986943, 4 more genes
    nsv4825840copy number variation1nstd200human GRCh37 chr8: 53,842,934-53,942,379 , GRCh38.p12 chr8: 52,930,374-53,029,819 LOC101060191, NPBWR1
    nsv4825832copy number variation1nstd200human GRCh37 chr8: 53,371,963-53,915,751 , GRCh38.p12 chr8: 52,459,403-53,003,191 ALKAL1, LOC101060191, 4 more genes
    nsv4729338copy number variation1nstd102humanUncertain significance GRCh37 chr8: 52,605,905-54,913,501 , GRCh38.p12 chr8: 51,693,345-54,000,941 RPL34P17, ATP6V1H, 26 more genes
    nsv4675047copy number variation1nstd102humanUncertain significance GRCh37 chr8: 53,383,339-53,856,239 , GRCh38.p12 chr8: 52,470,779-52,943,679 NPBWR1, RB1CC1, 3 more genes
    nsv4610367copy number variation1nstd183human GRCh37 chr8: 53,698,800-53,874,866 , GRCh38.p12 chr8: 52,786,240-52,962,306 LOC107986943, NPBWR1
    nsv4456871copy number variation1nstd102humanPathogenic GRCh37 chr8: 39,555,657-64,049,089 , GRCh38.p12 chr8: 39,698,138-63,136,530 CRIPTOP5, TRIM60P15, 297 more genes
    nsv4456811copy number variation1nstd102humanPathogenic GRCh37 chr8: 31,936,551-146,295,771 , GRCh38.p12 chr8: 32,079,035-145,070,385 TERF1, LOC107986945, 1511 more genes
    nsv4455130copy number variation1nstd102humanUncertain significance GRCh37 chr8: 53,548,484-54,017,118 , GRCh38.p12 chr8: 52,635,924-53,104,558 RB1CC1, LOC101060191, 3 more genes
    nsv4404690copy number variation1nstd174human GRCh37 chr8: 53,302,090-53,919,610 , GRCh38.p12 chr8: 52,389,530-53,007,050 NPBWR1, ST18, 5 more genes
    nsv4401209copy number variation1nstd174human GRCh37 chr8: 53,665,633-53,881,213 , GRCh38.p12 chr8: 52,753,073-52,968,653 LOC105375835, NPBWR1, 1 more genes
    nsv4394405copy number variation1nstd174human GRCh37 chr8: 53,845,174-53,943,853 , GRCh38.p12 chr8: 52,932,614-53,031,293 NPBWR1, LOC101060191
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