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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5960163insertion1nstd209human GRCh38 chr9: 130,176,169-130,176,169 , GRCh37.p13 chr9|NW_004070869.1: 45,599-45,599 , GRCh37.p13 chr9: 132,938,448-132,938,448 NCS1
    nsv5921158copy number variation1nstd209human GRCh38 chr9: 130,225,072-130,259,913 , GRCh37.p13 chr9: 132,987,351-133,022,192 , GRCh37.p13 chr9|NW_004070869.1: 94,502-129,343 NCS1, MIR12126
    nsv5919075copy number variation1nstd209human GRCh38 chr9: 130,213,637-130,215,650 , GRCh37.p13 chr9: 132,975,916-132,977,929 , GRCh37.p13 chr9|NW_004070869.1: 83,067-85,080 NCS1
    nsv5917863copy number variation1nstd209human GRCh38 chr9: 130,237,530-130,239,161 , GRCh37.p13 chr9: 132,999,809-133,001,440 , GRCh37.p13 chr9|NW_004070869.1: 106,960-108,591 NCS1
    nsv5867040copy number variation1nstd209human GRCh38 chr9: 130,178,641-130,185,582 , GRCh37.p13 chr9: 132,940,920-132,947,861 , GRCh37.p13 chr9|NW_004070869.1: 48,071-55,012 NCS1
    nsv5866699copy number variation1nstd209human GRCh38 chr9: 130,232,660-130,234,659 , GRCh37.p13 chr9|NW_004070869.1: 102,090-104,089 , GRCh37.p13 chr9: 132,994,939-132,996,938 NCS1
    nsv5866069copy number variation1nstd209human GRCh38 chr9: 130,178,541-130,183,501 , GRCh37.p13 chr9: 132,940,820-132,945,780 , GRCh37.p13 chr9|NW_004070869.1: 47,971-52,931 NCS1
    nsv5862258copy number variation2nstd209human GRCh38 chr9: 130,237,204-130,239,203 , GRCh37.p13 chr9|NW_004070869.1: 106,634-108,633 , GRCh37.p13 chr9: 132,999,483-133,001,482 NCS1
    nsv5860942copy number variation1nstd209human GRCh38 chr9: 130,224,756-130,231,859 , GRCh37.p13 chr9|NW_004070869.1: 94,186-101,289 , GRCh37.p13 chr9: 132,987,035-132,994,138 NCS1
    nsv5860568copy number variation1nstd209human GRCh38 chr9: 130,235,385-130,246,280 , GRCh37.p13 chr9|NW_004070869.1: 104,815-115,710 , GRCh37.p13 chr9: 132,997,664-133,008,559 NCS1, MIR12126
    nsv5857838copy number variation1nstd209human GRCh38 chr9: 130,172,254-130,174,356 , GRCh37.p13 chr9: 132,934,533-132,936,635 , GRCh37.p13 chr9|NW_004070869.1: 41,684-43,786 NCS1
    nsv5853957copy number variation1nstd209human GRCh38 chr9: 130,172,534-130,177,740 , GRCh37.p13 chr9|NW_004070869.1: 41,964-47,170 , GRCh37.p13 chr9: 132,934,813-132,940,019 NCS1
    nsv5852565copy number variation1nstd209human GRCh38 chr9: 130,213,727-130,215,826 , GRCh37.p13 chr9: 132,976,006-132,978,105 , GRCh37.p13 chr9|NW_004070869.1: 83,157-85,256 NCS1
    nsv5850928copy number variation1nstd209human GRCh38 chr9: 130,169,683-130,175,931 , GRCh37.p13 chr9|NW_004070869.1: 39,113-45,361 , GRCh37.p13 chr9: 132,931,962-132,938,210 NCS1
    nsv5632285insertion2nstd207human GRCh38 chr9: 130,221,881-130,221,881 , GRCh37.p13 chr9: 132,984,160-132,984,160 , GRCh37.p13 chr9|NW_004070869.1: 91,311-91,311 NCS1
    nsv5599546copy number variation1nstd207human GRCh38 chr9: 130,221,771-130,221,882 , GRCh37.p13 chr9|NW_004070869.1: 91,201-91,312 , GRCh37.p13 chr9: 132,984,050-132,984,161 NCS1
    nsv5477666copy number variation1nstd206human GRCh38 chr9: 130,189,749-130,191,114 , GRCh37.p13 chr9|NW_004070869.1: 59,179-60,544 , GRCh37.p13 chr9: 132,952,028-132,953,393 NCS1
    nsv5317520copy number variation1nstd204human GRCh37.p13 chr9: 133,223,037-133,497,604 , GRCh38.p13 chr9: 130,177,410-130,622,217 , ASS1, 7 more genes
    nsv5255663copy number variation1nstd204human GRCh38.p13 chr9: 130,177,141-130,250,493 , GRCh37.p13 chr9: 132,939,420-133,012,772 , GRCh37.p13 chr9|NW_004070869.1: 46,571-119,923 NCS1, MIR12126
    nsv5249935copy number variation1nstd204human GRCh38.p13 chr9: 130,192,346-130,194,645 , GRCh37.p13 chr9|NW_004070869.1: 61,776-64,075 , GRCh37.p13 chr9: 132,954,625-132,956,924 NCS1
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