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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5866315copy number variation1nstd209human GRCh38 chr11: 135,071,648-135,074,047 , GRCh37.p13 chr11: 134,941,542-134,943,941 LINC02684
    nsv5862556copy number variation1nstd209human GRCh38 chr11: 135,066,425-135,072,897 , GRCh37.p13 chr11: 134,936,319-134,942,791 LINC02684
    nsv5857140copy number variation1nstd209human GRCh38 chr11: 135,069,075-135,074,047 , GRCh37.p13 chr11: 134,938,969-134,943,941 LINC02684
    nsv5848002copy number variation1nstd209human GRCh38 chr11: 135,072,998-135,075,694 , GRCh37.p13 chr11: 134,942,892-134,945,588 LINC02684
    nsv5646269insertion1nstd207human GRCh38 chr11: 135,076,364-135,076,364 , GRCh37.p13 chr11: 134,946,258-134,946,258 LINC02684
    nsv5494009copy number variation1nstd206human GRCh38 chr11: 135,056,364-135,076,500 , GRCh37.p13 chr11: 134,926,258-134,946,394 LINC02684
    nsv5301766copy number variation1nstd204human GRCh38.p13 chr11: 135,075,697-135,076,374 , GRCh37.p13 chr11: 134,945,591-134,946,268 LINC02684
    nsv4974203copy number variation1nstd200human GRCh38 chr11: 135,068,878-135,073,594 , GRCh37.p13 chr11: 134,938,772-134,943,488 LINC02684
    nsv4844769copy number variation1nstd200human GRCh37 chr11: 134,936,141-134,941,438 , GRCh38.p12 chr11: 135,066,247-135,071,544 LINC02684
    nsv4673961copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,226,940-134,944,477 , GRCh38.p12 chr11: 124,357,044-135,074,583 OR8A2P, LOC101929473, 186 more genes
    nsv4656758copy number variation1nstd186human GRCh37 chr11: 134,946,393-134,946,457 , GRCh38.p12 chr11: 135,076,499-135,076,563 LINC02684
    nsv4655923copy number variation1nstd186human GRCh37 chr11: 134,946,366-134,946,459 , GRCh38.p12 chr11: 135,076,472-135,076,565 LINC02684
    nsv4606615copy number variation1nstd183human GRCh37 chr11: 134,908,185-134,943,360 , GRCh38.p12 chr11: 135,038,291-135,073,466 LINC02684
    nsv4600482copy number variation1nstd183human GRCh37 chr11: 134,921,483-134,944,770 , GRCh38.p12 chr11: 135,051,589-135,074,876 LINC02684
    nsv4599290copy number variation2nstd183human GRCh37 chr11: 134,848,428-134,940,871 , GRCh38.p12 chr11: 134,978,534-135,070,977 LINC02684, LOC105369587, 2 more genes
    nsv4598753copy number variation1nstd183human GRCh37 chr11: 134,893,273-134,943,360 , GRCh38.p12 chr11: 135,023,379-135,073,466 LINC02684
    nsv4527636copy number variation1nstd166human GRCh37.p13 chr11: 134,860,999-134,946,000 , GRCh38.p12 chr11: 134,991,105-135,076,106 LOC105369587, LINC02717, 1 more genes
    nsv4527411copy number variation1nstd166human GRCh37.p13 chr11: 134,946,366-134,946,459 , GRCh38.p12 chr11: 135,076,472-135,076,565 LINC02684
    nsv4527380copy number variation1nstd166human GRCh37.p13 chr11: 134,946,393-134,946,457 , GRCh38.p12 chr11: 135,076,499-135,076,563 LINC02684
    nsv4428106copy number variation1nstd174human GRCh37 chr11: 134,920,082-134,945,587 , GRCh38.p12 chr11: 135,050,188-135,075,693 LINC02684
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