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Items: 1 to 20 of 230

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5964594insertion1nstd209human GRCh38 chr1: 201,933,555-201,933,555 , GRCh37.p13 chr1: 201,902,683-201,902,683 LMOD1
    nsv5692452mobile element insertion2nstd211human GRCh38 chr1: 201,939,908-201,939,908 , GRCh37.p13 chr1: 201,909,036-201,909,036 LMOD1
    nsv5609123insertion1nstd207human GRCh38 chr1: 201,901,536-201,901,536 , GRCh37.p13 chr1: 201,870,664-201,870,664 LMOD1
    nsv5580735copy number variation1nstd207human GRCh38 chr1: 201,901,560-201,901,627 , GRCh37.p13 chr1: 201,870,688-201,870,755 LMOD1
    nsv5579727copy number variation1nstd207human GRCh38 chr1: 201,924,395-201,924,498 , GRCh37.p13 chr1: 201,893,523-201,893,626 LMOD1
    nsv5441172copy number variation1nstd206human GRCh38 chr1: 201,901,563-201,901,693 , GRCh37.p13 chr1: 201,870,691-201,870,821 LMOD1
    nsv5434637copy number variation1nstd206human GRCh38 chr1: 201,933,539-201,933,628 , GRCh37.p13 chr1: 201,902,667-201,902,756 LMOD1
    nsv5402078mobile element insertion1nstd206human GRCh38 chr1: 201,939,908-201,939,959 , GRCh37.p13 chr1: 201,909,036-201,909,087 LMOD1
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5063773mobile element insertion1nstd203human GRCh38 chr1: 201,936,310-201,936,310 , GRCh37.p13 chr1: 201,905,438-201,905,438 LMOD1
    nsv4891580copy number variation1nstd200human GRCh38 chr1: 201,928,994-201,935,745 , GRCh37.p13 chr1: 201,898,122-201,904,873 LMOD1
    nsv4891579copy number variation1nstd200human GRCh38 chr1: 201,902,072-201,902,688 , GRCh37.p13 chr1: 201,871,200-201,871,816 LMOD1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4748381copy number variation1nstd199human GRCh37 chr1: 201,870,652-201,870,718 , GRCh38.p12 chr1: 201,901,524-201,901,590 LMOD1
    nsv4742662copy number variation1nstd199human GRCh37 chr1: 201,893,540-201,893,641 , GRCh38.p12 chr1: 201,924,412-201,924,513 LMOD1
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 more genes
    nsv4460550mobile element insertion1nstd166human GRCh37.p13 chr1: 201,905,438-201,905,438 , GRCh38.p12 chr1: 201,936,310-201,936,310 LMOD1
    nsv4459902mobile element insertion1nstd166human GRCh37.p13 chr1: 201,891,401-201,891,401 , GRCh38.p12 chr1: 201,922,273-201,922,273 LMOD1
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
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