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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142014insertion1nstd232human GRCh37.p13 chr1: 167,511,537-167,511,537 , GRCh38.p12 chr1: 167,542,300-167,542,300 CREG1
    nsv7099244copy number variation1nstd231human GRCh38.p12 chr1: 166,864,890-169,028,321 , GRCh37 chr1: 166,834,127-168,997,559 CD247, DPT, 49 more genes
    nsv7095561copy number variation1nstd102humanUncertain significance GRCh37 chr1: 167,400,918-168,282,240 , GRCh38.p12 chr1: 167,431,681-168,313,002 GCSHP5, RNU6-1310P, 21 more genes
    nsv7039884inversion1nstd229human GRCh38 chr1: 159,817,036-167,858,499 , GRCh37.p13 chr1: 159,786,826-167,827,737 TRP-AGG2-1, FCGR2C, 228 more genes
    nsv6644239copy number variation1nstd229human GRCh38 chr1: 167,270,558-167,699,449 , GRCh37.p13 chr1: 167,239,795-167,668,686 POU2F1, LOC101928512, 6 more genes
    nsv6644130copy number variation1nstd229human GRCh38 chr1: 167,542,907-167,548,862 , GRCh37.p13 chr1: 167,512,144-167,518,099 CREG1
    nsv6643754copy number variation1nstd229human GRCh38 chr1: 167,550,602-167,553,335 , GRCh37.p13 chr1: 167,519,839-167,522,572 CREG1
    nsv6643753copy number variation1nstd229human GRCh38 chr1: 167,542,299-167,546,098 , GRCh37.p13 chr1: 167,511,536-167,515,335 CREG1
    nsv6625670copy number variation1nstd224human GRCh37 chr1: 167,507,857-167,562,816 , GRCh38.p12 chr1: 167,538,620-167,593,579 CREG1, RPS18P4
    nsv6540250inversion1nstd223human GRCh38 chr1: 163,441,141-169,028,378 , GRCh37.p13 chr1: 163,410,931-168,997,616 LOC107985452, NMNAT1P2, 96 more genes
    nsv6324790copy number variation1nstd223human GRCh38 chr1: 167,544,001-167,546,200 , GRCh37.p13 chr1: 167,513,238-167,515,437 CREG1
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133597copy number variation1nstd213human GRCh37 chr1: 167,470,000-170,370,001 , GRCh38.p12 chr1: 167,500,763-170,400,860 CD247, XCL1, 64 more genes
    nsv6133565copy number variation1nstd213human GRCh37 chr1: 164,310,000-170,640,001 , GRCh38.p12 chr1: 164,340,763-170,670,860 ATP1B1, DPT, 126 more genes
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5041452inversion1nstd200human GRCh38 chr1: 163,441,139-169,028,376 , GRCh37.p13 chr1: 163,410,929-168,997,614 , RPS17P6, 97 more genes
    nsv4897912copy number variation1nstd200human GRCh38 chr1: 167,550,768-167,550,891 , GRCh37.p13 chr1: 167,520,005-167,520,128 CREG1
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
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