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Items: 1 to 20 of 35

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673475copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,362,414-158,409,266 , GRCh38.p12 chr3: 158,644,625-158,691,477 LXN, GFM1
    nsv7096701copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,376,701-158,409,266 , GRCh38.p12 chr3: 158,658,912-158,691,477 LXN, GFM1
    nsv5673558copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,380,407-158,384,185 , GRCh38.p12 chr3: 158,662,618-158,666,396 LXN, GFM1
    nsv3880729copy number variation1nstd102humanBenign GRCh37 chr3: 158,342,928-158,411,681 , GRCh38.p12 chr3: 158,625,139-158,693,892 LXN, GFM1
    nsv3877682copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,361,184-158,410,354 , GRCh38.p12 chr3: 158,643,395-158,692,565 LXN, GFM1
    nsv7096942copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,362,424-158,409,256 , GRCh38.p12 chr3: 158,644,635-158,691,467 LXN, GFM1
    nsv7137159copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,384,176-158,410,362 , GRCh38.p12 chr3: 158,666,387-158,692,573 LXN, GFM1
    nsv6289964copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,305,597-158,428,584 , GRCh38.p12 chr3: 158,587,808-158,710,795 LXN, MTAPP1, 3 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LXN, LOC102724145, 273 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 LXN, RNU4-62P, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 LXN, NDUFB4, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 LXN, RPL23AP49, 2875 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LXN, LINC02614, 1469 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 LXN, H1-10, 846 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LXN, LOC105374179, 785 more genes
    nsv3874894copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426 LXN, RNU6-901P, 673 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 LXN, LOC105374260, 696 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 LXN, LINC02031, 647 more genes
    nsv3913128copy number variation1nstd102humanPathogenic GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323 LXN, SNORA4, 644 more genes
    nsv3914686copy number variation1nstd102humanPathogenic NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727 LXN, RPL34P10, 625 more genes
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