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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5684289mobile element insertion2nstd211human GRCh38 chr2: 207,755,971-207,755,971 , GRCh37.p13 chr2: 208,620,695-208,620,695 FZD5, CCNYL1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5412535mobile element insertion1nstd206human GRCh38 chr2: 207,755,971-207,756,022 , GRCh37.p13 chr2: 208,620,695-208,620,746 FZD5, CCNYL1
    nsv5318715copy number variation1nstd204human GRCh38.p13 chr2: 207,759,076-207,765,612 , GRCh37.p13 chr2: 208,623,800-208,630,336 FZD5
    nsv5217052copy number variation1nstd204human GRCh38.p13 chr2: 207,759,059-207,765,540 , GRCh37.p13 chr2: 208,623,783-208,630,264 FZD5
    nsv5079578mobile element insertion1nstd203human GRCh38 chr2: 207,757,825-207,757,839 , GRCh37.p13 chr2: 208,622,549-208,622,563 FZD5
    nsv5070014mobile element insertion1nstd203human GRCh38 chr2: 207,757,276-207,757,289 , GRCh37.p13 chr2: 208,622,000-208,622,013 FZD5
    nsv5063504mobile element insertion1nstd203human GRCh38 chr2: 207,755,954-207,755,971 , GRCh37.p13 chr2: 208,620,678-208,620,695 CCNYL1, FZD5
    nsv5033412inversion1nstd200human GRCh38 chr2: 206,107,842-207,979,103 , GRCh37.p13 chr2: 206,972,566-208,843,827 ATP5POP1, MIR2355, 39 more genes
    nsv4916513copy number variation1nstd200human GRCh38 chr2: 207,759,081-207,765,609 , GRCh37.p13 chr2: 208,623,805-208,630,333 FZD5
    nsv4913874copy number variation1nstd200human GRCh38 chr2: 207,765,014-207,765,210 , GRCh37.p13 chr2: 208,629,738-208,629,934 FZD5
    nsv4876881inversion1nstd200human GRCh37 chr2: 206,972,566-208,843,827 , GRCh38.p12 chr2: 206,107,842-207,979,103 CREB1, RN7SKP260, 39 more genes
    nsv4804576copy number variation1nstd200human GRCh37 chr2: 208,629,738-208,629,934 , GRCh38.p12 chr2: 207,765,014-207,765,210 FZD5
    nsv4795704copy number variation1nstd200human GRCh37 chr2: 208,623,805-208,630,333 , GRCh38.p12 chr2: 207,759,081-207,765,609 FZD5
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728545copy number variation1nstd102humanPathogenic GRCh37 chr2: 204,445,619-212,580,788 , GRCh38.p12 chr2: 203,580,896-211,716,063 FASTKD2, MYL6BP1, 110 more genes
    nsv4674383copy number variation1nstd102humanPathogenic GRCh37 chr2: 163,233,162-211,927,188 , GRCh38.p12 chr2: 162,376,652-211,062,464 SNORA41, LOC101929633, 663 more genes
    nsv4554908insertion1nstd166human GRCh37.p13 chr2: 208,620,678-208,620,678 , GRCh38.p12 chr2: 207,755,954-207,755,954 FZD5, CCNYL1
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4316119inversion1nstd166human GRCh37.p13 chr2: 187,130,612-218,396,189 , GRCh38.p12 chr2: 186,265,885-217,531,466 , ACADL, 453 more genes
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