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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5953560insertion1nstd209human GRCh38 chr1: 209,697,884-209,697,884 , GRCh37.p13 chr1: 209,871,229-209,871,229 HSD11B1, HSD11B1-AS1
    nsv5886652copy number variation1nstd209human GRCh38 chr1: 209,671,501-209,671,564 , GRCh37.p13 chr1: 209,844,846-209,844,909 HSD11B1-AS1
    nsv5884149copy number variation1nstd209human GRCh38 chr1: 209,681,473-209,683,406 , GRCh37.p13 chr1: 209,854,818-209,856,751 HSD11B1-AS1
    nsv5828879copy number variation1nstd209human GRCh38 chr1: 209,681,470-209,683,169 , GRCh37.p13 chr1: 209,854,815-209,856,514 HSD11B1-AS1
    nsv5583160copy number variation1nstd207human GRCh38 chr1: 209,671,501-209,671,564 , GRCh37.p13 chr1: 209,844,846-209,844,909 HSD11B1-AS1
    nsv5446177copy number variation1nstd206human GRCh38 chr1: 209,671,504-209,671,565 , GRCh37.p13 chr1: 209,844,849-209,844,910 HSD11B1-AS1
    nsv5445175copy number variation1nstd206human GRCh38 chr1: 209,681,475-209,683,407 , GRCh37.p13 chr1: 209,854,820-209,856,752 HSD11B1-AS1
    nsv5385123copy number variation1nstd186human GRCh37 chr1: 209,844,849-209,844,910 , GRCh38.p12 chr1: 209,671,504-209,671,565 HSD11B1-AS1
    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
    nsv5283990copy number variation1nstd204human GRCh38.p13 chr1: 209,671,504-209,671,565 , GRCh37.p13 chr1: 209,844,849-209,844,910 HSD11B1-AS1
    nsv5192777mobile element insertion1nstd203human GRCh38 chr1: 209,690,994-209,690,994 , GRCh37.p13 chr1: 209,864,339-209,864,339 HSD11B1-AS1, HSD11B1
    nsv5075218mobile element insertion1nstd203human GRCh38 chr1: 209,685,530-209,685,540 , GRCh37.p13 chr1: 209,858,875-209,858,885 HSD11B1, HSD11B1-AS1
    nsv5074552mobile element insertion1nstd203human GRCh38 chr1: 209,719,019-209,719,019 , GRCh37.p13 chr1: 209,892,364-209,892,364 HSD11B1, HSD11B1-AS1
    nsv5069148mobile element insertion1nstd203human GRCh38 chr1: 209,697,884-209,697,914 , GRCh37.p13 chr1: 209,871,229-209,871,259 HSD11B1, HSD11B1-AS1
    nsv5060863mobile element insertion1nstd203human GRCh38 chr1: 209,683,548-209,683,564 , GRCh37.p13 chr1: 209,856,893-209,856,909 HSD11B1-AS1
    nsv4904304copy number variation1nstd200human GRCh38 chr1: 209,737,845-209,765,280 , GRCh37.p13 chr1: 209,911,190-209,938,625 ADORA2BP1, HSD11B1-AS1, 1 more genes
    nsv4898462copy number variation1nstd200human GRCh38 chr1: 209,673,293-209,673,402 , GRCh37.p13 chr1: 209,846,638-209,846,747 HSD11B1-AS1
    nsv4898461copy number variation1nstd200human GRCh38 chr1: 209,671,504-209,671,565 , GRCh37.p13 chr1: 209,844,849-209,844,910 HSD11B1-AS1
    nsv4898460copy number variation1nstd200human GRCh38 chr1: 209,659,030-209,667,281 , GRCh37.p13 chr1: 209,832,375-209,840,626 HSD11B1-AS1
    nsv4898459copy number variation1nstd200human GRCh38 chr1: 209,658,673-209,662,540 , GRCh37.p13 chr1: 209,832,018-209,835,885 HSD11B1-AS1
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