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Items: 1 to 20 of 580

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv6657170copy number variation1nstd229human GRCh38 chr1: 919,548-919,602 , GRCh37.p13 chr1: 854,928-854,982 LOC107985728, LINC02593
    nsv6657155copy number variation1nstd229human GRCh38 chr1: 917,002-957,005 , GRCh37.p13 chr1: 852,382-892,385 LOC107985728, LINC02593, 2 more genes
    nsv6657054copy number variation1nstd229human GRCh38 chr1: 912,717-930,843 , GRCh37.p13 chr1: 848,097-866,223 LOC284600, SAMD11, 2 more genes
    nsv6656896copy number variation1nstd229human GRCh38 chr1: 905,159-917,775 , GRCh37.p13 chr1: 840,539-853,155 LINC02593, LOC284600
    nsv6656706copy number variation1nstd229human GRCh38 chr1: 872,115-945,244 , GRCh37.p13 chr1: 807,495-880,624 LINC02593, NOC2L, 5 more genes
    nsv6656705copy number variation1nstd229human GRCh38 chr1: 872,040-1,151,798 , GRCh37.p13 chr1: 807,420-1,087,178 C1orf159, LOC105378948, 17 more genes
    nsv6656432copy number variation1nstd229human GRCh38 chr1: 860,901-1,011,800 , GRCh37.p13 chr1: 796,281-947,180 NOC2L, LOC284600, 12 more genes
    nsv6656330copy number variation1nstd229human GRCh38 chr1: 846,209-955,066 , GRCh37.p13 chr1: 781,589-890,446 SAMD11, LINC01128, 7 more genes
    nsv6656142copy number variation1nstd229human GRCh38 chr1: 838,653-1,166,615 , GRCh37.p13 chr1: 774,033-1,101,995 LINC01128, SAMD11, 21 more genes
    nsv6655873copy number variation1nstd229human GRCh38 chr1: 829,470-1,107,141 , GRCh37.p13 chr1: 764,850-1,042,521 LOC107985728, PERM1, 18 more genes
    nsv6655607copy number variation1nstd229human GRCh38 chr1: 818,880-922,261 , GRCh37.p13 chr1: 754,260-857,641 LOC107985728, FAM87B, 7 more genes
    nsv6655052copy number variation1nstd229human GRCh38 chr1: 818,999-1,165,510 , GRCh37.p13 chr1: 754,379-1,100,890 HES4, LOC105378948, 22 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636416copy number variation1nstd102humanUncertain significance GRCh37 chr1: 849,467-1,174,365 , GRCh38.p12 chr1: 914,087-1,238,985 RNF223, SAMD11, 24 more genes
    nsv6636292copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-2,972,435 , GRCh38.p12 chr1: 914,087-3,055,871 LOC105378602, LOC105378599, 108 more genes
    nsv6626514copy number variation1nstd224human GRCh37 chr1: 752,566-909,917 , GRCh38.p12 chr1: 817,186-974,537 LINC00115, LINC02593, 12 more genes
    nsv6626467copy number variation5nstd224human GRCh37 chr1: 727,841-851,390 , GRCh38.p12 chr1: 792,461-916,010 LINC00115, FAM41C, 7 more genes
    nsv6626395copy number variation1nstd224human GRCh37 chr1: 752,566-866,438 , GRCh38.p12 chr1: 817,186-931,058 LINC00115, FAM41C, 8 more genes
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