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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893027copy number variation1nstd209human GRCh38 chr4: 119,944,367-119,945,445 , GRCh37.p13 chr4: 120,865,522-120,866,600 LINC02502
    nsv5837639copy number variation1nstd209human GRCh38 chr4: 119,944,373-119,945,472 , GRCh37.p13 chr4: 120,865,528-120,866,627 LINC02502
    nsv5718979mobile element insertion1nstd211human GRCh38 chr4: 119,948,437-119,948,437 , GRCh37.p13 chr4: 120,869,592-120,869,592 LINC02502
    nsv5570553copy number variation1nstd207human GRCh38 chr4: 119,944,367-119,945,442 , GRCh37.p13 chr4: 120,865,522-120,866,597 LINC02502
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5467952copy number variation1nstd206human GRCh38 chr4: 119,944,367-119,945,450 , GRCh37.p13 chr4: 120,865,522-120,866,605 LINC02502
    nsv5386424copy number variation2nstd186human GRCh37 chr4: 120,865,522-120,866,605 , GRCh38.p12 chr4: 119,944,367-119,945,450 LINC02502
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv5311564copy number variation1nstd204human GRCh38.p13 chr4: 119,944,367-119,945,450 , GRCh37.p13 chr4: 120,865,522-120,866,605 LINC02502
    nsv5235303copy number variation1nstd204human GRCh38.p13 chr4: 119,944,373-119,945,472 , GRCh37.p13 chr4: 120,865,528-120,866,627 LINC02502
    nsv5221222copy number variation1nstd204human GRCh38.p13 chr4: 119,944,401-119,945,400 , GRCh37.p13 chr4: 120,865,556-120,866,555 LINC02502
    nsv4935561copy number variation1nstd200human GRCh38 chr4: 119,944,367-119,945,450 , GRCh37.p13 chr4: 120,865,522-120,866,605 LINC02502
    nsv4808204copy number variation1nstd200human GRCh37 chr4: 120,865,522-120,866,605 , GRCh38.p12 chr4: 119,944,367-119,945,450 LINC02502
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4749198copy number variation1nstd199human GRCh37 chr4: 120,865,515-120,866,589 , GRCh38.p12 chr4: 119,944,360-119,945,434 LINC02502
    nsv4658899copy number variation1nstd186human GRCh37 chr4: 120,865,522-120,866,605 , GRCh38.p12 chr4: 119,944,367-119,945,450 LINC02502
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