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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
    nsv5921764copy number variation1nstd209human GRCh38 chr10: 80,134,710-80,134,833 , GRCh37.p13 chr10: 81,894,466-81,894,589 PLAC9
    nsv5911808copy number variation1nstd209human GRCh38 chr10: 80,135,060-80,135,365 , GRCh37.p13 chr10: 81,894,816-81,895,121 PLAC9
    nsv5909992copy number variation1nstd209human GRCh38 chr10: 72,964,663-80,533,256 , GRCh37.p13 chr10: 74,724,421-82,293,012 , PRXL2A, 155 more genes
    nsv5672415inversion1nstd207human GRCh38 chr10: 79,542,902-80,213,948 , GRCh37.p13 chr10: 81,302,658-81,973,704 , ANXA11, 30 more genes
    nsv5563886sequence alteration1nstd206human GRCh38 chr10: 79,543,104-80,217,086 , GRCh37.p13 chr10: 81,302,860-81,976,842 , ANXA11, 30 more genes
    nsv5492266copy number variation1nstd206human GRCh38 chr10: 80,112,988-80,135,627 , GRCh37.p13 chr10: 81,872,744-81,895,383 PLAC9, RPL22P18
    nsv5490020copy number variation1nstd206human GRCh38 chr10: 80,130,945-80,138,784 , GRCh37.p13 chr10: 81,890,701-81,898,540 PLAC9
    nsv5483974copy number variation1nstd206human GRCh38 chr10: 79,796,368-80,226,368 , GRCh37.p13 chr10: 81,556,124-81,986,124 LOC642361, C1DP2, 20 more genes
    nsv5479685copy number variation1nstd206human GRCh38 chr10: 79,846,368-80,228,368 , GRCh37.p13 chr10: 81,606,124-81,988,124 ZNRF2P3, LINC00857, 18 more genes
    nsv5475024copy number variation1nstd206human GRCh38 chr10: 80,135,060-80,135,366 , GRCh37.p13 chr10: 81,894,816-81,895,122 PLAC9
    nsv5249336copy number variation1nstd204human GRCh38.p13 chr10: 80,133,400-80,172,936 , GRCh37.p13 chr10: 81,893,156-81,932,692 PLAC9, ANXA11
    nsv5128561mobile element insertion1nstd203human GRCh38 chr10: 80,135,361-80,135,366 , GRCh37.p13 chr10: 81,895,117-81,895,122 PLAC9
    nsv5030933inversion1nstd200human GRCh38 chr10: 57,233,666-95,028,660 , GRCh37.p13 chr10: 58,993,426-96,788,417 , RNU6-740P, 615 more genes
    nsv4976755copy number variation1nstd200human GRCh38 chr10: 80,135,469-80,135,603 , GRCh37.p13 chr10: 81,895,225-81,895,359 PLAC9
    nsv4976754copy number variation1nstd200human GRCh38 chr10: 80,134,539-80,135,575 , GRCh37.p13 chr10: 81,894,295-81,895,331 PLAC9
    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
    nsv4729258copy number variation1nstd102humanUncertain significance GRCh37 chr10: 81,457,752-81,990,746 , GRCh38.p12 chr10: 79,697,996-80,230,990 RPL22P18, MBL1P, 21 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
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