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Items: 1 to 20 of 487

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960720insertion1nstd209human GRCh38 chr4: 176,767,097-176,767,097 , GRCh37.p13 chr4: 177,688,251-177,688,251 VEGFC
    nsv5906290copy number variation1nstd209human GRCh38 chr4: 176,770,416-176,770,670 , GRCh37.p13 chr4: 177,691,570-177,691,824 VEGFC
    nsv5901087copy number variation1nstd209human GRCh38 chr4: 176,739,940-176,739,999 , GRCh37.p13 chr4: 177,661,094-177,661,153 VEGFC
    nsv5838453copy number variation1nstd209human GRCh38 chr4: 176,777,972-176,780,071 , GRCh37.p13 chr4: 177,699,126-177,701,225 VEGFC
    nsv5717995mobile element insertion1nstd211human GRCh38 chr4: 176,692,231-176,692,231 , GRCh37.p13 chr4: 177,613,385-177,613,385 VEGFC, HAFML
    nsv5683947mobile element insertion2nstd211human GRCh38 chr4: 176,692,418-176,692,418 , GRCh37.p13 chr4: 177,613,572-177,613,572 HAFML, VEGFC
    nsv5627426insertion1nstd207human GRCh38 chr4: 176,740,449-176,740,449 , GRCh37.p13 chr4: 177,661,603-177,661,603 VEGFC
    nsv5578081copy number variation1nstd207human GRCh38 chr4: 176,739,940-176,739,999 , GRCh37.p13 chr4: 177,661,094-177,661,153 VEGFC
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5472870copy number variation1nstd206human GRCh38 chr4: 176,734,472-176,734,530 , GRCh37.p13 chr4: 177,655,626-177,655,684 VEGFC
    nsv5471346copy number variation1nstd206human GRCh38 chr4: 176,768,503-176,768,859 , GRCh37.p13 chr4: 177,689,657-177,690,013 VEGFC
    nsv5464067copy number variation1nstd206human GRCh38 chr4: 176,752,077-176,758,839 , GRCh37.p13 chr4: 177,673,231-177,679,993 VEGFC
    nsv5457199copy number variation1nstd206human GRCh38 chr4: 176,736,218-176,739,851 , GRCh37.p13 chr4: 177,657,372-177,661,005 VEGFC
    nsv5455458copy number variation1nstd206human GRCh38 chr4: 176,792,836-176,792,894 , GRCh37.p13 chr4: 177,713,990-177,714,048 VEGFC
    nsv5454398copy number variation1nstd206human GRCh38 chr4: 176,770,416-176,770,671 , GRCh37.p13 chr4: 177,691,570-177,691,825 VEGFC
    nsv5361998translocation1nstd200human GRCh38 chr4: 176,792,894-176,792,894 , GRCh38 chr4: 176,792,836-176,792,836 , GRCh37.p13 chr4: 177,714,048-177,714,048 , GRCh37.p13 chr4: 177,713,990-177,713,990 VEGFC
    nsv5361997translocation1nstd200human GRCh38 chr4: 176,770,671-176,770,671 , GRCh38 chr4: 176,770,416-176,770,416 , GRCh37.p13 chr4: 177,691,570-177,691,570 , GRCh37.p13 chr4: 177,691,825-177,691,825 VEGFC
    nsv5361996translocation1nstd200human GRCh38 chr4: 176,758,069-176,758,069 , GRCh38 chr4: 176,758,135-176,758,135 , GRCh37.p13 chr4: 177,679,289-177,679,289 , GRCh37.p13 chr4: 177,679,223-177,679,223 VEGFC
    nsv5340578translocation1nstd200human GRCh37 chr4: 177,714,048-177,714,048 , GRCh37 chr4: 177,713,990-177,713,990 , GRCh38.p12 chr4: 176,792,836-176,792,836 , GRCh38.p12 chr4: 176,792,894-176,792,894 VEGFC
    nsv5337133translocation1nstd200human GRCh37 chr4: 177,691,570-177,691,570 , GRCh37 chr4: 177,691,825-177,691,825 , GRCh38.p12 chr4: 176,770,416-176,770,416 , GRCh38.p12 chr4: 176,770,671-176,770,671 VEGFC
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