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Items: 1 to 20 of 322

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966126insertion1nstd209human GRCh38 chr6: 110,837,735-110,837,735 , GRCh37.p13 chr6: 111,158,938-111,158,938 AMD1
    nsv5896699copy number variation1nstd209human GRCh38 chr6: 110,862,536-110,865,462 , GRCh37.p13 chr6: 111,183,739-111,186,665 AMD1
    nsv5844308copy number variation2nstd209human GRCh38 chr6: 110,862,982-110,864,081 , GRCh37.p13 chr6: 111,184,185-111,185,284 AMD1
    nsv5844215copy number variation1nstd209human GRCh38 chr6: 110,862,639-110,865,481 , GRCh37.p13 chr6: 111,183,842-111,186,684 AMD1
    nsv5689551mobile element insertion1nstd211human GRCh38 chr6: 110,855,089-110,855,089 , GRCh37.p13 chr6: 111,176,292-111,176,292 AMD1, RNU6-1115P
    nsv5676425mobile element insertion1nstd211human GRCh38 chr6: 110,816,561-110,816,561 , GRCh37.p13 chr6: 111,137,764-111,137,764 CDK19, AMD1
    nsv5634757insertion1nstd207human GRCh38 chr6: 110,857,542-110,857,542 , GRCh37.p13 chr6: 111,178,745-111,178,745 CNN2P9, AMD1
    nsv5564516copy number variation1nstd102humanUncertain significance GRCh37 chr6: 109,796,301-113,083,437 , GRCh38.p12 chr6: 109,475,098-112,762,235 RN7SL617P, METTL24, 67 more genes
    nsv5469677copy number variation1nstd206human GRCh38 chr6: 110,728,014-110,822,490 , GRCh37.p13 chr6: 111,049,217-111,143,693 AMD1, CDK19
    nsv5468148copy number variation1nstd206human GRCh38 chr6: 110,832,241-110,835,328 , GRCh37.p13 chr6: 111,153,444-111,156,531 AMD1
    nsv5466146copy number variation1nstd206human GRCh38 chr6: 110,874,507-110,874,581 , GRCh37.p13 chr6: 111,195,710-111,195,784 AMD1
    nsv5465217copy number variation1nstd206human GRCh38 chr6: 110,847,374-110,848,350 , GRCh37.p13 chr6: 111,168,577-111,169,553 SNORA40C, AMD1
    nsv5461742copy number variation1nstd206human GRCh38 chr6: 110,881,391-110,917,703 , GRCh37.p13 chr6: 111,202,594-111,238,906 AMD1
    nsv5461262copy number variation1nstd206human GRCh38 chr6: 110,842,266-110,842,383 , GRCh37.p13 chr6: 111,163,469-111,163,586 AMD1
    nsv5456071copy number variation1nstd206human GRCh38 chr6: 110,893,065-110,893,472 , GRCh37.p13 chr6: 111,214,268-111,214,675 AMD1
    nsv5454545copy number variation1nstd206human GRCh38 chr6: 110,892,346-110,892,796 , GRCh37.p13 chr6: 111,213,549-111,213,999 AMD1
    nsv5400984mobile element insertion1nstd206human GRCh38 chr6: 110,816,561-110,816,612 , GRCh37.p13 chr6: 111,137,764-111,137,815 AMD1, CDK19
    nsv5369244translocation1nstd200human GRCh38 chr6: 14,639,665-14,639,665 , GRCh38 chr6: 110,893,627-110,893,627 , GRCh37.p13 chr6: 111,214,830-111,214,830 , GRCh37.p13 chr6: 14,639,896-14,639,896 AMD1, LOC101928354
    nsv5311712copy number variation1nstd204human GRCh37.p13 chr6: 111,168,573-111,169,517 , GRCh38.p13 chr6: 110,847,370-110,848,314 SNORA40C, AMD1
    nsv5301703copy number variation1nstd204human GRCh38.p13 chr6: 110,825,864-110,827,976 , GRCh37.p13 chr6: 111,147,067-111,149,179 AMD1
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