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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5867098copy number variation2nstd209human GRCh38 chr10: 80,246,288-80,248,511 , GRCh37.p13 chr10: 82,006,044-82,008,267 LOC100130698, EIF5AP4
    nsv5860013copy number variation2nstd209human GRCh38 chr10: 80,240,169-80,245,951 , GRCh37.p13 chr10: 81,999,925-82,005,707 LOC100130698, EIF5AP4
    nsv5637311insertion1nstd207human GRCh38 chr10: 80,252,598-80,252,598 , GRCh37.p13 chr10: 82,012,354-82,012,354 LOC100130698
    nsv5489050copy number variation1nstd206human GRCh38 chr10: 80,251,105-80,251,333 , GRCh37.p13 chr10: 82,010,861-82,011,089 LOC100130698
    nsv5487955copy number variation1nstd206human GRCh38 chr10: 80,251,503-80,251,592 , GRCh37.p13 chr10: 82,011,259-82,011,348 LOC100130698
    nsv5484738copy number variation1nstd206human GRCh38 chr10: 80,226,917-80,250,026 , GRCh37.p13 chr10: 81,986,673-82,009,782 LOC100130698, EIF5AP4
    nsv5477656copy number variation1nstd206human GRCh38 chr10: 80,239,368-80,251,868 , GRCh37.p13 chr10: 81,999,124-82,011,624 EIF5AP4, LOC100130698
    nsv5259389copy number variation1nstd204human GRCh38.p13 chr10: 80,249,501-80,250,100 , GRCh37.p13 chr10: 82,009,257-82,009,856 LOC100130698
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4729484copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,457,752-89,253,430 , GRCh38.p12 chr10: 79,697,996-87,493,673 DPY19L2P5, TSPAN14-AS1, 115 more genes
    nsv4729317copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,617,260-89,146,780 , GRCh38.p12 chr10: 79,857,504-87,387,023 LOC105378390, LRIT1, 109 more genes
    nsv4729182copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,028,088-82,059,110 , GRCh38.p12 chr10: 79,268,331-80,299,354 SFTPA1, RPS12P18, 40 more genes
    nsv4728963copy number variation1nstd102humanUncertain significance GRCh37 chr10: 82,008,644-82,210,730 , GRCh38.p12 chr10: 80,248,888-80,450,974 ZNF519P1, MAT1A, 4 more genes
    nsv4728260copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,585,301-89,101,700 , GRCh38.p12 chr10: 79,825,545-87,341,943 C1DP3, RNA5SP322, 109 more genes
    nsv4680846copy number variation1nstd189human GRCh37.p13 chr10: 81,906,297-82,259,340 , GRCh38.p12 chr10: 80,146,541-80,499,584 ANXA11, MAT1A, 9 more genes
    nsv4644243copy number variation1nstd186human GRCh37 chr10: 82,002,000-82,009,200 , GRCh38.p12 chr10: 80,242,244-80,249,444 LOC100130698, EIF5AP4
    nsv4456843copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,858,697-82,127,631 , GRCh38.p12 chr10: 80,098,941-80,367,875 LOC100130698, RPL22P18, 9 more genes
    nsv4349613copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,697,811-88,768,847 , GRCh38.p12 chr10: 79,938,055-87,009,090 MIR346, LOC101929662, 91 more genes
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