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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6676108copy number variation1nstd229human GRCh38 chr2: 46,805,907-46,821,455 , GRCh37.p13 chr2: 47,033,046-47,048,594 LINC01118
    nsv6675836copy number variation1nstd229human GRCh38 chr2: 46,816,531-46,851,012 , GRCh37.p13 chr2: 47,043,670-47,078,151 LINC01118, LOC107985880, 1 more genes
    nsv6674980copy number variation1nstd229human GRCh38 chr2: 46,822,656-46,951,505 , GRCh37.p13 chr2: 47,049,795-47,178,644 LINC01119, TTC7A, 3 more genes
    nsv6673730copy number variation1nstd229human GRCh38 chr2: 46,783,756-46,839,430 , GRCh37.p13 chr2: 47,010,895-47,066,569 LINC01118, LINC01119
    nsv6671611copy number variation1nstd229human GRCh38 chr2: 46,818,579-46,829,127 , GRCh37.p13 chr2: 47,045,718-47,056,266 LINC01119, LINC01118
    nsv6667033copy number variation1nstd229human GRCh38 chr2: 46,794,650-46,829,928 , GRCh37.p13 chr2: 47,021,789-47,057,067 LINC01118, LINC01119
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6352405copy number variation1nstd223human GRCh38 chr2: 46,805,907-46,821,451 , GRCh37.p13 chr2: 47,033,046-47,048,590 LINC01118
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6137693copy number variation1nstd102humannot provided GRCh38 chr2: 46,722,010-46,985,532 , GRCh37.p13 chr2: 46,949,149-47,212,671 TTC7A, LINC01119, 4 more genes
    nsv6134459copy number variation1nstd213human GRCh37 chr2: 40,080,000-50,820,001 , GRCh38.p12 chr2: 39,852,860-50,592,863 , BCYRN1, 149 more genes
    nsv6134458copy number variation2nstd213human GRCh37 chr2: 38,440,000-47,670,001 , GRCh38.p12 chr2: 38,212,858-47,442,862 ASS1P2, BCYRN1, 144 more genes
    nsv6134457copy number variation1nstd213human GRCh37 chr2: 38,410,000-75,540,001 , GRCh38.p12 chr2: 38,182,858-75,312,875 , ACTG2, 598 more genes
    nsv5878103copy number variation1nstd209human GRCh38 chr2: 46,809,931-46,818,240 , GRCh37.p13 chr2: 47,037,070-47,045,379 LINC01118
    nsv5832685copy number variation1nstd209human GRCh38 chr2: 46,809,921-46,817,355 , GRCh37.p13 chr2: 47,037,060-47,044,494 LINC01118
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv4908623copy number variation1nstd200human GRCh38 chr2: 46,724,036-46,817,628 , GRCh37.p13 chr2: 46,951,175-47,044,767 SOCS5, LINC01118
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