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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926874copy number variation1nstd209human GRCh38 chr10: 103,171,796-103,173,354 , GRCh37.p13 chr10: 104,931,553-104,933,111 NT5C2
    nsv5912740copy number variation1nstd209human GRCh38 chr10: 103,158,816-103,174,096 , GRCh37.p13 chr10: 104,918,573-104,933,853 NT5C2, MARCKSL1P1
    nsv5862625copy number variation1nstd209human GRCh38 chr10: 103,172,185-103,173,484 , GRCh37.p13 chr10: 104,931,942-104,933,241 MARCKSL1P1, NT5C2
    nsv5644073insertion1nstd207human GRCh38 chr10: 103,183,275-103,183,275 , GRCh37.p13 chr10: 104,943,032-104,943,032 NT5C2
    nsv5638136insertion1nstd207human GRCh38 chr10: 103,129,763-103,129,763 , GRCh37.p13 chr10: 104,889,520-104,889,520 NT5C2
    nsv5634077insertion1nstd207human GRCh38 chr10: 103,129,622-103,129,622 , GRCh37.p13 chr10: 104,889,379-104,889,379 NT5C2
    nsv5591136copy number variation1nstd207human GRCh38 chr10: 103,129,890-103,129,940 , GRCh37.p13 chr10: 104,889,647-104,889,697 NT5C2
    nsv5544219insertion1nstd206human GRCh38 chr10: 103,151,315-103,151,352 , GRCh37.p13 chr10: 104,911,072-104,911,109 NT5C2
    nsv5504854copy number variation1nstd206human GRCh38 chr10: 103,138,428-103,138,499 , GRCh37.p13 chr10: 104,898,185-104,898,256 NT5C2
    nsv5503907copy number variation1nstd206human GRCh38 chr10: 103,124,218-103,124,374 , GRCh37.p13 chr10: 104,883,975-104,884,131 NT5C2, RPS15AP29
    nsv5499968copy number variation1nstd206human GRCh38 chr10: 103,172,971-103,173,993 , GRCh37.p13 chr10: 104,932,728-104,933,750 NT5C2, MARCKSL1P1
    nsv5499838copy number variation1nstd206human GRCh38 chr10: 103,167,064-103,248,547 , GRCh37.p13 chr10: 104,926,821-105,008,304 RPEL1, MARCKSL1P1, 2 more genes
    nsv5318868copy number variation1nstd204human GRCh37.p13 chr10: 104,932,717-104,933,758 , GRCh38.p13 chr10: 103,172,960-103,174,001 NT5C2, MARCKSL1P1
    nsv5258856copy number variation1nstd204human GRCh38.p13 chr10: 103,099,401-103,103,800 , GRCh37.p13 chr10: 104,859,158-104,863,557 NT5C2
    nsv5185617mobile element insertion1nstd203human GRCh38 chr10: 103,172,208-103,172,219 , GRCh37.p13 chr10: 104,931,965-104,931,976 NT5C2
    nsv5180852mobile element insertion1nstd203human GRCh38 chr10: 103,147,192-103,147,204 , GRCh37.p13 chr10: 104,906,949-104,906,961 NT5C2
    nsv5120479mobile element insertion1nstd203human GRCh38 chr10: 103,114,217-103,114,250 , GRCh37.p13 chr10: 104,873,974-104,874,007 NT5C2
    nsv4970388copy number variation1nstd200human GRCh38 chr10: 103,172,968-103,173,994 , GRCh37.p13 chr10: 104,932,725-104,933,751 NT5C2, MARCKSL1P1
    nsv4970387copy number variation1nstd200human GRCh38 chr10: 103,135,858-103,228,663 , GRCh37.p13 chr10: 104,895,615-104,988,420 NT5C2, MARCKSL1P1, 1 more genes
    nsv4970386copy number variation1nstd200human GRCh38 chr10: 103,114,405-103,116,402 , GRCh37.p13 chr10: 104,874,162-104,876,159 NT5C2
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