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Items: 1 to 20 of 159

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5610235insertion1nstd207human GRCh38 chr4: 42,110,060-42,110,060 , GRCh37.p13 chr4: 42,112,077-42,112,077 BEND4
    nsv5459038copy number variation1nstd206human GRCh38 chr4: 42,119,538-42,119,694 , GRCh37.p13 chr4: 42,121,555-42,121,711 BEND4
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5037441inversion1nstd200human GRCh38 chr4: 42,118,031-42,118,233 , GRCh37.p13 chr4: 42,120,048-42,120,250 BEND4
    nsv4928521copy number variation1nstd200human GRCh38 chr4: 42,140,236-42,140,463 , GRCh37.p13 chr4: 42,142,253-42,142,480 BEND4
    nsv4928520copy number variation1nstd200human GRCh38 chr4: 42,133,708-42,135,561 , GRCh37.p13 chr4: 42,135,725-42,137,578 BEND4
    nsv4928519copy number variation1nstd200human GRCh38 chr4: 42,128,886-42,130,407 , GRCh37.p13 chr4: 42,130,903-42,132,424 BEND4
    nsv4791578copy number variation1nstd200human GRCh37 chr4: 42,142,253-42,142,480 , GRCh38.p12 chr4: 42,140,236-42,140,463 BEND4
    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
    nsv4684161copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881 TLR10, WDR1, 669 more genes
    nsv4591021copy number variation1nstd183human GRCh37 chr4: 42,105,897-42,117,622 , GRCh38.p12 chr4: 42,103,880-42,115,605 BEND4
    nsv4475519mobile element insertion1nstd166human GRCh37.p13 chr4: 42,148,968-42,148,968 , GRCh38.p12 chr4: 42,146,951-42,146,951 BEND4
    nsv4322375inversion1nstd166human GRCh37.p13 chr4: 42,120,000-42,120,250 , GRCh38.p12 chr4: 42,117,983-42,118,233 BEND4
    nsv4102886copy number variation1nstd166human GRCh37.p13 chr4: 42,123,087-42,123,242 , GRCh38.p12 chr4: 42,121,070-42,121,225 BEND4
    nsv4102811copy number variation1nstd166human GRCh37.p13 chr4: 42,142,253-42,142,480 , GRCh38.p12 chr4: 42,140,236-42,140,463 BEND4
    nsv3923949copy number variation1nstd102humanPathogenic GRCh37 chr4: 40,498,493-49,581,867 , NCBI36 chr4: 40,193,250-49,276,624 , GRCh38 chr4: 40,496,476-49,579,850 CWH43, LOC100419154, 104 more genes
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