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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094386copy number variation1nstd102humanUncertain significance GRCh37 chr15: 51,687,012-51,748,586 , GRCh38.p12 chr15: 51,394,815-51,456,389 DMXL2, GLDN
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6977090copy number variation1nstd229human GRCh38 chr15: 51,360,201-51,526,100 , GRCh37.p13 chr15: 51,652,398-51,818,297 GLDN, DMXL2
    nsv6976802copy number variation1nstd229human GRCh38 chr15: 51,355,897-51,426,480 , GRCh37.p13 chr15: 51,648,094-51,718,677 GLDN
    nsv6976299copy number variation1nstd229human GRCh38 chr15: 51,368,128-51,373,092 , GRCh37.p13 chr15: 51,660,325-51,665,289 GLDN
    nsv6974837copy number variation1nstd229human GRCh38 chr15: 51,283,672-51,364,165 , GRCh37.p13 chr15: 51,575,869-51,656,362 CYP19A1, MIR7973-2, 4 more genes
    nsv6974522copy number variation1nstd229human GRCh38 chr15: 51,386,515-51,456,594 , GRCh37.p13 chr15: 51,678,712-51,748,791 DMXL2, GLDN
    nsv6973390copy number variation1nstd229human GRCh38 chr15: 51,408,334-51,456,395 , GRCh37.p13 chr15: 51,700,531-51,748,592 GLDN, DMXL2
    nsv6971157copy number variation1nstd229human GRCh38 chr15: 51,384,383-51,456,604 , GRCh37.p13 chr15: 51,676,580-51,748,801 DMXL2, GLDN
    nsv6970391copy number variation1nstd229human GRCh38 chr15: 51,375,906-51,379,090 , GRCh37.p13 chr15: 51,668,103-51,671,287 GLDN
    nsv6968891copy number variation1nstd229human GRCh38 chr15: 51,336,065-51,386,085 , GRCh37.p13 chr15: 51,628,262-51,678,282 GLDN, CYP19A1
    nsv6968250copy number variation1nstd229human GRCh38 chr15: 51,355,931-51,464,485 , GRCh37.p13 chr15: 51,648,128-51,756,682 GLDN, DMXL2
    nsv6966364copy number variation1nstd229human GRCh38 chr15: 51,333,255-51,446,945 , GRCh37.p13 chr15: 51,625,452-51,739,142 DMXL2, GLDN, 1 more genes
    nsv6963920copy number variation1nstd229human GRCh38 chr15: 50,582,205-51,473,799 , GRCh37.p13 chr15: 50,874,402-51,765,996 RN7SL354P, DCAF13P3, 13 more genes
    nsv6962052copy number variation1nstd229human GRCh38 chr15: 50,611,455-51,586,706 , GRCh37.p13 chr15: 50,903,652-51,878,903 SPPL2A, CYP19A1, 13 more genes
    nsv6961594copy number variation1nstd229human GRCh38 chr15: 51,351,580-51,361,088 , GRCh37.p13 chr15: 51,643,777-51,653,285 GLDN
    nsv6637724copy number variation1nstd102humanUncertain significance GRCh37 chr15: 51,464,187-51,675,037 , GRCh38.p12 chr15: 51,171,990-51,382,840 MIR4713, CYP19A1, 5 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
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