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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924292copy number variation1nstd209human GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828 LHX6, MORN5
    nsv5640866insertion1nstd207human GRCh38 chr9: 122,191,048-122,191,048 , GRCh37.p13 chr9: 124,953,327-124,953,327 LHX6, MORN5
    nsv5634759insertion1nstd207human GRCh38 chr9: 122,185,417-122,185,417 , GRCh37.p13 chr9: 124,947,696-124,947,696 LHX6, MORN5
    nsv5631269insertion1nstd207human GRCh38 chr9: 122,189,561-122,189,561 , GRCh37.p13 chr9: 124,951,840-124,951,840 LHX6, MORN5
    nsv5604518copy number variation1nstd207human GRCh38 chr9: 122,185,417-122,185,549 , GRCh37.p13 chr9: 124,947,696-124,947,828 LHX6, MORN5
    nsv5476659copy number variation1nstd206human GRCh38 chr9: 122,229,067-122,229,261 , GRCh37.p13 chr9: 124,991,346-124,991,540 LHX6
    nsv5135340mobile element insertion1nstd203human GRCh38 chr9: 122,185,467-122,185,478 , GRCh37.p13 chr9: 124,947,746-124,947,757 MORN5, LHX6
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4675789copy number variation1nstd102humanUncertain significance GRCh37 chr9: 124,604,592-126,306,080 , GRCh38.p12 chr9: 121,842,313-123,543,801 MIR7150, OR1N2, 43 more genes
    nsv4614978copy number variation1nstd183human GRCh37 chr9: 124,975,871-124,988,688 , GRCh38.p12 chr9: 122,213,592-122,226,409 LHX6
    nsv4493169mobile element insertion1nstd166human GRCh37.p13 chr9: 124,960,849-124,960,849 , GRCh38.p12 chr9: 122,198,570-122,198,570 MORN5, LHX6
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4181463copy number variation1nstd166human GRCh37.p13 chr9: 124,984,477-124,984,561 , GRCh38.p12 chr9: 122,222,198-122,222,282 LHX6
    nsv4176582copy number variation1nstd166human GRCh37.p13 chr9: 124,991,319-124,991,540 , GRCh38.p12 chr9: 122,229,040-122,229,261 LHX6
    nsv3966729copy number variation1nstd168human GRCh38 chr9: 122,171,494-122,191,692 , GRCh37.p13 chr9: 124,933,773-124,953,971 MORN5, LHX6
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 more genes
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