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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960443insertion1nstd209human GRCh38 chr2: 200,516,616-200,516,616 , GRCh37.p13 chr2: 201,381,339-201,381,339 SGO2
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5538491insertion1nstd206human GRCh38 chr2: 200,516,616-200,516,667 , GRCh37.p13 chr2: 201,381,339-201,381,390 SGO2
    nsv5444500copy number variation1nstd206human GRCh38 chr2: 200,554,051-200,555,765 , GRCh37.p13 chr2: 201,418,774-201,420,488 SGO2
    nsv4910294copy number variation1nstd200human GRCh38 chr2: 200,566,940-200,567,978 , GRCh37.p13 chr2: 201,431,663-201,432,701 SGO2
    nsv4910293copy number variation1nstd200human GRCh38 chr2: 200,561,587-200,584,444 , GRCh37.p13 chr2: 201,426,310-201,449,167 AOX1, SGO2
    nsv4910292copy number variation1nstd200human GRCh38 chr2: 200,535,965-200,539,164 , GRCh37.p13 chr2: 201,400,688-201,403,887 SGO2
    nsv4795514copy number variation1nstd200human GRCh37 chr2: 201,431,663-201,432,701 , GRCh38.p12 chr2: 200,566,940-200,567,978 SGO2
    nsv4795513copy number variation1nstd200human GRCh37 chr2: 201,426,310-201,449,167 , GRCh38.p12 chr2: 200,561,587-200,584,444 SGO2, AOX1
    nsv4795512copy number variation1nstd200human GRCh37 chr2: 201,400,688-201,403,887 , GRCh38.p12 chr2: 200,535,965-200,539,164 SGO2
    nsv4768322copy number variation1nstd102humanPathogenic GRCh37 chr2: 197,359,024-201,383,462 , GRCh38.p12 chr2: 196,494,300-200,518,739 ANKRD44-DT, ATP5MC2P3, 48 more genes
    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
    nsv4674597copy number variation1nstd102humanPathogenic GRCh37 chr2: 201,106,432-204,901,548 , GRCh38.p12 chr2: 200,241,709-204,036,825 KIAA2012-AS1, SNORD11, 113 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
    nsv4571109mobile element insertion1nstd166human GRCh37.p13 chr2: 201,408,328-201,408,328 , GRCh38.p12 chr2: 200,543,605-200,543,605 SGO2
    nsv4550165insertion1nstd166human GRCh37.p13 chr2: 201,381,339-201,381,339 , GRCh38.p12 chr2: 200,516,616-200,516,616 SGO2
    nsv4519699copy number variation1nstd166human GRCh37.p13 chr2: 201,426,153-201,429,691 , GRCh38.p12 chr2: 200,561,430-200,564,968 SGO2
    nsv4518538copy number variation1nstd166human GRCh37.p13 chr2: 201,410,102-201,639,125 , GRCh38.p12 chr2: 200,545,379-200,774,402 AOX1, SGO2, 5 more genes
    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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