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Items: 1 to 20 of 228

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979070insertion1nstd209human GRCh38 chr15: 65,542,066-65,542,066 , GRCh37.p13 chr15: 65,834,404-65,834,404 HACD3
    nsv5944999copy number variation1nstd209human GRCh38 chr15: 65,539,813-65,539,866 , GRCh37.p13 chr15: 65,832,151-65,832,204 HACD3
    nsv5514147copy number variation1nstd206human GRCh38 chr15: 65,534,874-65,544,874 , GRCh37.p13 chr15: 65,827,212-65,837,212 HACD3
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5301129copy number variation1nstd204human GRCh38.p13 chr15: 65,524,435-65,533,974 , GRCh37.p13 chr15: 65,816,773-65,826,312 HACD3
    nsv5279689copy number variation1nstd204human GRCh38.p13 chr15: 65,526,613-65,534,141 , GRCh37.p13 chr15: 65,818,951-65,826,479 HACD3
    nsv5272140copy number variation1nstd204human GRCh38.p13 chr15: 65,522,201-65,529,000 , GRCh37.p13 chr15: 65,814,539-65,821,338 HACD3
    nsv5265020copy number variation1nstd204human GRCh38.p13 chr15: 65,524,401-65,534,000 , GRCh37.p13 chr15: 65,816,739-65,826,338 HACD3
    nsv5159244mobile element insertion1nstd203human GRCh38 chr15: 65,531,567-65,531,582 , GRCh37.p13 chr15: 65,823,905-65,823,920 HACD3
    nsv5146245mobile element insertion1nstd203human GRCh38 chr15: 65,542,066-65,542,083 , GRCh37.p13 chr15: 65,834,404-65,834,421 HACD3
    nsv5143002mobile element insertion1nstd203human GRCh38 chr15: 65,573,760-65,573,772 , GRCh37.p13 chr15: 65,866,098-65,866,110 HACD3
    nsv4992061copy number variation1nstd200human GRCh38 chr15: 65,524,445-65,533,949 , GRCh37.p13 chr15: 65,816,783-65,826,287 HACD3
    nsv4849875copy number variation1nstd200human GRCh37 chr15: 65,834,423-65,835,200 , GRCh38.p12 chr15: 65,542,085-65,542,862 HACD3
    nsv4849874copy number variation1nstd200human GRCh37 chr15: 65,816,783-65,826,287 , GRCh38.p12 chr15: 65,524,445-65,533,949 HACD3
    nsv4755691insertion1nstd199human GRCh37 chr15: 65,834,416-65,834,416 , GRCh38.p12 chr15: 65,542,078-65,542,078 HACD3
    nsv4428550copy number variation1nstd174human GRCh37 chr15: 65,810,201-65,822,252 , GRCh38.p12 chr15: 65,517,863-65,529,914 DPP8, HACD3
    nsv4245235copy number variation1nstd166human GRCh37.p13 chr15: 65,869,870-65,869,935 , GRCh38.p12 chr15: 65,577,532-65,577,597 INTS14, HACD3
    nsv4241668copy number variation1nstd166human GRCh37.p13 chr15: 65,828,122-65,833,521 , GRCh38.p12 chr15: 65,535,784-65,541,183 HACD3
    nsv3955674copy number variation1nstd168human GRCh38 chr15: 65,484,679-65,530,009 , GRCh37.p13 chr15: 65,777,017-65,822,347 DPP8, HACD3
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
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