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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5473247copy number variation1nstd206human GRCh38 chr4: 151,089,131-151,200,368 , GRCh37.p13 chr4: 152,010,283-152,121,520 RPS3A, SNORD73A, 4 more genes
    nsv4948563copy number variation1nstd200human GRCh38 chr4: 150,745,207-151,150,945 , GRCh37.p13 chr4: 151,666,359-152,072,097 SH3D19, AK4P6, 6 more genes
    nsv4948562copy number variation1nstd200human GRCh38 chr4: 150,733,429-151,295,714 , GRCh37.p13 chr4: 151,654,581-152,216,866 AK4P6, PRSS48, 8 more genes
    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
    nsv4680623copy number variation1nstd189human GRCh37.p13 chr4: 151,680,492-152,079,299 , GRCh38.p12 chr4: 150,759,340-151,158,147 LRBA, RPS3A, 6 more genes
    nsv4680372copy number variation1nstd189human GRCh37.p13 chr4: 151,668,147-152,044,738 , GRCh38.p12 chr4: 150,746,995-151,123,586 LRBA, RPS3A, 6 more genes
    nsv4679738copy number variation1nstd189human GRCh37.p13 chr4: 151,668,147-152,071,888 , GRCh38.p12 chr4: 150,746,995-151,150,736 LRBA, RPS3A, 6 more genes
    nsv4596951copy number variation1nstd183human GRCh37 chr4: 151,693,149-152,071,888 , GRCh38.p12 chr4: 150,771,997-151,150,736 LRBA, RPS3A, 6 more genes
    nsv4587612copy number variation1nstd183human GRCh37 chr4: 151,795,520-153,192,881 , GRCh38.p12 chr4: 150,874,368-152,271,729 RPS3A, RNA5SP169, 22 more genes
    nsv4522180copy number variation1nstd166human GRCh37.p13 chr4: 151,830,999-152,071,000 , GRCh38.p12 chr4: 150,909,847-151,149,848 LRBA, RPS3A, 6 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
    nsv4400300copy number variation1nstd174human GRCh37 chr4: 151,664,438-152,071,888 , GRCh38.p12 chr4: 150,743,286-151,150,736 LRBA, RPS3A, 6 more genes
    nsv4388092copy number variation1nstd173human GRCh37 chr4: 151,668,146-152,071,875 , GRCh38.p12 chr4: 150,746,994-151,150,723 LRBA, RPS3A, 6 more genes
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