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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978280inversion1nstd209human GRCh38 chr15: 50,713,517-50,714,395 , GRCh37.p13 chr15: 51,005,714-51,006,592 SPPL2A
    nsv5937679copy number variation1nstd209human GRCh38 chr15: 50,754,838-50,755,040 , GRCh37.p13 chr15: 51,047,035-51,047,237 SPPL2A
    nsv5933379copy number variation1nstd209human GRCh38 chr15: 50,725,552-50,928,408 , GRCh37.p13 chr15: 51,017,749-51,220,605 AP4E1, SPPL2A, 1 more genes
    nsv5930039copy number variation1nstd209human GRCh38 chr15: 50,476,256-50,892,576 , GRCh37.p13 chr15: 50,768,453-51,184,773 , USP8, 5 more genes
    nsv5865235copy number variation1nstd209human GRCh38 chr15: 50,679,467-50,729,311 , GRCh37.p13 chr15: 50,971,664-51,021,508 TRPM7, SPPL2A, 1 more genes
    nsv5858981copy number variation2nstd209human GRCh38 chr15: 50,725,263-50,885,692 , GRCh37.p13 chr15: 51,017,460-51,177,889 RPL32P30, SPPL2A
    nsv5858346copy number variation2nstd209human GRCh38 chr15: 50,727,412-50,729,011 , GRCh37.p13 chr15: 51,019,609-51,021,208 SPPL2A
    nsv5847664copy number variation2nstd209human GRCh38 chr15: 50,727,512-50,730,611 , GRCh37.p13 chr15: 51,019,709-51,022,808 SPPL2A
    nsv5714007mobile element insertion1nstd211human GRCh38 chr15: 50,730,005-50,730,005 , GRCh37.p13 chr15: 51,022,202-51,022,202 SPPL2A
    nsv5651829insertion1nstd207human GRCh38 chr15: 50,720,517-50,720,517 , GRCh37.p13 chr15: 51,012,714-51,012,714 SPPL2A
    nsv5554862inversion1nstd206human GRCh38 chr15: 50,712,828-50,714,829 , GRCh37.p13 chr15: 51,005,025-51,007,026 SPPL2A
    nsv5530696copy number variation1nstd206human GRCh38 chr15: 50,759,268-50,764,167 , GRCh37.p13 chr15: 51,051,465-51,056,364 SPPL2A
    nsv5528496copy number variation1nstd206human GRCh38 chr15: 50,737,574-50,739,349 , GRCh37.p13 chr15: 51,029,771-51,031,546 SPPL2A
    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
    nsv5357915translocation1nstd200human GRCh38 chr15: 50,755,668-50,755,668 , GRCh38 chr15: 50,755,556-50,755,556 , GRCh37.p13 chr15: 51,047,753-51,047,753 , GRCh37.p13 chr15: 51,047,865-51,047,865 SPPL2A
    nsv5357914translocation1nstd200human GRCh38 chr15: 50,723,818-50,723,818 , GRCh38 chr15: 50,723,764-50,723,764 , GRCh37.p13 chr15: 51,015,961-51,015,961 , GRCh37.p13 chr15: 51,016,015-51,016,015 SPPL2A
    nsv5330835translocation1nstd200human GRCh37 chr15: 51,015,961-51,015,961 , GRCh37 chr15: 51,016,015-51,016,015 , GRCh38.p12 chr15: 50,723,764-50,723,764 , GRCh38.p12 chr15: 50,723,818-50,723,818 SPPL2A
    nsv5315646copy number variation1nstd204human GRCh38.p13 chr15: 50,749,550-50,787,521 , GRCh37.p13 chr15: 51,041,747-51,079,718 SPPL2A
    nsv5303682copy number variation1nstd204human GRCh38.p13 chr15: 50,764,405-50,818,109 , GRCh37.p13 chr15: 51,056,602-51,110,306 RPL32P30, SPPL2A
    nsv5276667copy number variation1nstd204human GRCh38.p13 chr15: 50,749,501-50,787,500 , GRCh37.p13 chr15: 51,041,698-51,079,697 SPPL2A
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