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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6119901copy number variation1nstd186human GRCh37 chr6: 32,172,904-32,175,044 , GRCh38.p12 chr6: 32,205,127-32,207,267 NOTCH4
    nsv5888523copy number variation1nstd209human GRCh38 chr6: 32,205,125-32,207,266 , GRCh37.p13 chr6: 32,172,902-32,175,043 NOTCH4
    nsv5845236copy number variation1nstd209human GRCh38 chr6: 32,205,110-32,207,310 , GRCh37.p13 chr6: 32,172,887-32,175,087 NOTCH4
    nsv5454297copy number variation1nstd206human GRCh38 chr6: 32,205,127-32,207,267 , GRCh37.p13 chr6: 32,172,904-32,175,044 NOTCH4
    nsv5362820translocation1nstd200human GRCh38 chr6: 32,207,267-32,207,267 , GRCh38 chr6: 32,205,127-32,205,127 , GRCh37.p13 chr6: 32,175,044-32,175,044 , GRCh37.p13 chr6: 32,172,904-32,172,904 NOTCH4
    nsv5335362translocation1nstd200human GRCh37 chr6: 32,175,044-32,175,044 , GRCh37 chr6: 32,172,904-32,172,904 , GRCh38.p12 chr6: 32,207,267-32,207,267 , GRCh38.p12 chr6: 32,205,127-32,205,127 NOTCH4
    nsv5314332copy number variation1nstd204human GRCh38.p13 chr6: 32,205,117-32,207,276 , GRCh37.p13 chr6: 32,172,894-32,175,053 NOTCH4
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5231391copy number variation1nstd204human GRCh37.p13 chr6: 32,145,178-32,165,377 , GRCh38.p13 chr6: 32,177,401-32,197,600 AGER, NOTCH4, 5 more genes
    nsv5230008copy number variation1nstd204human GRCh38.p13 chr6: 32,205,110-32,207,110 , GRCh37.p13 chr6: 32,172,887-32,174,887 NOTCH4
    nsv5192416mobile element insertion1nstd203human GRCh38 chr6: 32,193,118-32,193,125 , GRCh37.p13 chr6: 32,160,895-32,160,902 NOTCH4, GPSM3
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
    nsv4728016copy number variation1nstd197human GRCh38.p12 chr6: 32,204,138-32,212,627 , GRCh37 chr6: 32,171,915-32,180,404 NOTCH4
    nsv4675941copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055 AGER, AIF1, 217 more genes
    nsv4675453copy number variation1nstd102humanUncertain significance GRCh37 chr6: 31,916,915-32,278,000 , GRCh38.p12 chr6: 31,949,138-32,310,223 NOTCH4, CYP21A2, 29 more genes
    nsv4662127copy number variation1nstd186human GRCh37 chr6: 32,172,902-32,175,044 , GRCh38.p12 chr6: 32,205,125-32,207,267 NOTCH4
    nsv4655114copy number variation1nstd186human GRCh37 chr6: 32,172,903-32,175,047 , GRCh38.p12 chr6: 32,205,126-32,207,270 NOTCH4
    nsv4592299copy number variation1nstd183human GRCh37 chr6: 32,172,902-32,175,044 , GRCh38.p12 chr6: 32,205,125-32,207,267 NOTCH4
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