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Items: 1 to 20 of 652

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117259mobile element insertion1nstd186human GRCh37 chr14: 62,283,731-62,283,746 , GRCh38.p12 chr14: 61,817,013-61,817,028 SYT16
    nsv6116904mobile element insertion1nstd186human GRCh37 chr14: 62,287,901-62,287,952 , GRCh38.p12 chr14: 61,821,183-61,821,234 SYT16
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5979551insertion1nstd209human GRCh38 chr14: 61,966,087-61,966,087 , GRCh37.p13 chr14: 62,432,805-62,432,805 SYT16
    nsv5979444insertion1nstd209human GRCh38 chr14: 61,821,164-61,821,164 , GRCh37.p13 chr14: 62,287,882-62,287,882 SYT16
    nsv5945744copy number variation1nstd209human GRCh38 chr14: 61,904,944-61,905,354 , GRCh37.p13 chr14: 62,371,662-62,372,072 SYT16
    nsv5943357copy number variation1nstd209human GRCh38 chr14: 62,046,086-62,046,327 , GRCh37.p13 chr14: 62,512,804-62,513,045 SYT16
    nsv5930621copy number variation1nstd209human GRCh38 chr14: 61,931,090-61,942,817 , GRCh37.p13 chr14: 62,397,808-62,409,535 SYT16
    nsv5928626copy number variation1nstd209human GRCh38 chr14: 61,878,742-61,878,791 , GRCh37.p13 chr14: 62,345,460-62,345,509 SYT16
    nsv5928215copy number variation1nstd209human GRCh38 chr14: 61,826,068-61,827,131 , GRCh37.p13 chr14: 62,292,786-62,293,849 SYT16
    nsv5863246copy number variation2nstd209human GRCh38 chr14: 61,932,013-61,933,112 , GRCh37.p13 chr14: 62,398,731-62,399,830 SYT16
    nsv5854457copy number variation2nstd209human GRCh38 chr14: 61,934,197-61,935,196 , GRCh37.p13 chr14: 62,400,915-62,401,914 SYT16
    nsv5854002copy number variation1nstd209human GRCh38 chr14: 62,006,564-62,007,663 , GRCh37.p13 chr14: 62,473,282-62,474,381 SYT16
    nsv5848660copy number variation1nstd209human GRCh38 chr14: 61,930,913-61,939,229 , GRCh37.p13 chr14: 62,397,631-62,405,947 SYT16
    nsv5847750copy number variation1nstd209human GRCh38 chr14: 61,826,099-61,827,098 , GRCh37.p13 chr14: 62,292,817-62,293,816 SYT16
    nsv5729342mobile element insertion1nstd211human GRCh38 chr14: 61,984,076-61,984,076 , GRCh37.p13 chr14: 62,450,794-62,450,794 SYT16
    nsv5712873mobile element insertion2nstd211human GRCh38 chr14: 62,022,852-62,022,852 , GRCh37.p13 chr14: 62,489,570-62,489,570 SYT16
    nsv5710315mobile element insertion2nstd211human GRCh38 chr14: 61,821,183-61,821,183 , GRCh37.p13 chr14: 62,287,901-62,287,901 SYT16
    nsv5707027mobile element insertion1nstd211human GRCh38 chr14: 61,841,492-61,841,492 , GRCh37.p13 chr14: 62,308,210-62,308,210 SYT16
    nsv5704101mobile element insertion1nstd211human GRCh38 chr14: 61,817,011-61,817,011 , GRCh37.p13 chr14: 62,283,729-62,283,729 SYT16
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