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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5673639copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,399,774-158,402,467 , GRCh38.p12 chr3: 158,681,985-158,684,678 GFM1
    nsv7096702copy number variation1nstd102humanPathogenic GRCh37 chr3: 158,407,942-158,409,266 , GRCh38.p12 chr3: 158,690,153-158,691,477 GFM1
    nsv4453105copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 158,399,774-158,409,266 , GRCh38 chr3: 158,681,985-158,691,477 GFM1
    nsv6311611copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 158,370,576-158,371,133 , GRCh38 chr3: 158,652,787-158,653,344 GFM1
    nsv7096545copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,399,764-158,409,256 , GRCh38.p12 chr3: 158,681,975-158,691,467 GFM1
    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 GFM1, LXN
    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 GFM1, LXN
    nsv6289964copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,305,597-158,428,584 , GRCh38.p12 chr3: 158,587,808-158,710,795 MTAPP1, RARRES1, 3 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3880617copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391 RPL23AP49, DLEC1, 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 LINC02614, LINC02054, 1469 more genes
    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
    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 LOC105374179, LINC02038, 785 more genes
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