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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5716093mobile element insertion1nstd211human GRCh38 chr1: 204,651,015-204,651,015 , GRCh37.p13 chr1: 204,620,143-204,620,143 LRRN2
    nsv5450662copy number variation1nstd206human GRCh38 chr1: 204,590,681-204,627,884 , GRCh37.p13 chr1: 204,559,809-204,597,012 LOC105371692, LRRN2
    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
    nsv5348056translocation1nstd200human GRCh38 chr1: 204,650,481-204,650,481 , GRCh38 chr1: 204,652,192-204,652,192 , GRCh37.p13 chr1: 204,621,320-204,621,320 , GRCh37.p13 chr1: 204,619,609-204,619,609 LRRN2
    nsv4891691copy number variation1nstd200human GRCh38 chr1: 204,653,894-204,674,501 , GRCh37.p13 chr1: 204,623,022-204,643,629 LRRN2
    nsv4891690copy number variation1nstd200human GRCh38 chr1: 204,638,877-204,640,443 , GRCh37.p13 chr1: 204,608,005-204,609,571 LRRN2
    nsv4891689copy number variation1nstd200human GRCh38 chr1: 204,631,681-204,633,654 , GRCh37.p13 chr1: 204,600,809-204,602,782 LRRN2
    nsv4789324copy number variation1nstd200human GRCh37 chr1: 204,623,022-204,643,629 , GRCh38.p12 chr1: 204,653,894-204,674,501 LRRN2
    nsv4789323copy number variation1nstd200human GRCh37 chr1: 204,619,608-204,621,324 , GRCh38.p12 chr1: 204,650,480-204,652,196 LRRN2
    nsv4789322copy number variation1nstd200human GRCh37 chr1: 204,608,005-204,609,571 , GRCh38.p12 chr1: 204,638,877-204,640,443 LRRN2
    nsv4789321copy number variation1nstd200human GRCh37 chr1: 204,600,809-204,602,782 , GRCh38.p12 chr1: 204,631,681-204,633,654 LRRN2
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 RNA5S8, NTPCR, 893 more genes
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
    nsv4380342copy number variation1nstd173human GRCh37 chr1: 204,625,007-204,647,493 , GRCh38.p12 chr1: 204,655,879-204,678,365 LRRN2
    nsv4378727copy number variation1nstd173human GRCh37 chr1: 204,624,957-204,647,493 , GRCh38.p12 chr1: 204,655,829-204,678,365 LRRN2
    nsv4069501copy number variation1nstd166human GRCh37.p13 chr1: 204,619,609-204,621,320 , GRCh38.p12 chr1: 204,650,481-204,652,192 LRRN2
    nsv4057604copy number variation1nstd166human GRCh37.p13 chr1: 204,625,236-204,637,614 , GRCh38.p12 chr1: 204,656,108-204,668,486 LRRN2
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