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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5957731insertion1nstd209human GRCh38 chr1: 145,842,809-145,842,809 , GRCh37.p13 chr1|NW_003871055.3: 2,658,222-2,658,222 , GRCh37.p13 chr1: 145,592,301-145,592,301 POLR3C
    nsv5885134copy number variation1nstd209human GRCh38 chr1: 143,707,729-148,368,205 , GRCh37.p13 chr1|NW_003871055.3: 523,142-5,183,618 , TRN-GTT22-1, 183 more genes
    nsv5881371copy number variation1nstd209human GRCh38 chr1: 145,648,753-147,971,330 , GRCh37.p13 chr1|NW_003871055.3: 2,464,166-4,786,743 , RNVU1-6, 72 more genes
    nsv5828105copy number variation2nstd209human GRCh38 chr1: 145,812,070-145,821,415 , GRCh37.p13 chr1|NW_003871055.3: 2,627,483-2,636,828 , GRCh37.p13 chr1: 145,613,690-145,623,022 POLR3C, RNF115
    nsv5675438mobile element insertion1nstd211human GRCh38 chr1: 145,843,506-145,843,506 , GRCh37.p13 chr1|NW_003871055.3: 2,658,919-2,658,919 , GRCh37.p13 chr1: 145,591,562-145,591,562 POLR3C, NUDT17
    nsv5564405copy number variation4nstd102humanPathogenic, Uncertain significance GRCh37 chr1: 145,414,782-145,610,584 , GRCh38.p12 chr1: 145,824,529-146,020,231 MIR6736, POLR3GL, 15 more genes
    nsv5425631copy number variation1nstd206human GRCh38 chr1: 145,563,293-146,185,587 , GRCh37.p13 chr1|NW_003871055.3: 2,378,706-3,001,000 , POLR3C, 29 more genes
    nsv5401406mobile element insertion1nstd206human GRCh38 chr1: 145,843,506-145,843,557 , GRCh37.p13 chr1|NW_003871055.3: 2,658,919-2,658,970 , GRCh37.p13 chr1: 145,591,511-145,591,562 NUDT17, POLR3C
    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
    nsv5216022copy number variation1nstd204human GRCh38.p13 chr1: 145,819,522-145,822,211 , GRCh37.p13 chr1|NW_003871055.3: 2,634,935-2,637,624 , GRCh37.p13 chr1: 145,612,897-145,615,583 POLR3C, RNF115
    nsv5210917copy number variation1nstd204human GRCh38.p13 chr1: 145,799,780-145,821,415 , GRCh37.p13 chr1: 145,613,690-145,635,298 , GRCh37.p13 chr1|NW_003871055.3: 2,615,193-2,636,828 RNF115, POLR3C
    nsv5206275copy number variation1nstd204human GRCh38.p13 chr1: 145,821,201-145,821,700 , GRCh37.p13 chr1|NW_003871055.3: 2,636,614-2,637,113 , GRCh37.p13 chr1: 145,613,408-145,613,904 RNF115, POLR3C
    nsv5202411copy number variation1nstd204human GRCh38.p13 chr1: 145,822,312-145,843,467 , GRCh37.p13 chr1: 145,591,601-145,612,796 , GRCh37.p13 chr1|NW_003871055.3: 2,637,725-2,658,880 POLR3C, NUDT17, 1 more genes
    nsv5201750copy number variation1nstd204human GRCh38.p13 chr1: 145,811,101-145,822,500 , GRCh37.p13 chr1|NW_003871055.3: 2,626,514-2,637,913 , GRCh37.p13 chr1: 145,612,609-145,623,984 RNF115, POLR3C
    nsv5201603copy number variation1nstd204human GRCh38.p13 chr1: 145,564,501-146,056,900 , GRCh37.p13 chr1|NW_003871055.3: 2,379,914-2,872,313 , GRCh37.p13 chr1: 145,382,661-145,833,118 , LINC01719, 27 more genes
    nsv5200304copy number variation1nstd102humanPathogenic GRCh37 chr1: 146,500,972-147,851,297 , GRCh38.p12 chr1: 145,430,980-148,371,305 RN7SL261P, LOC105371235, 103 more genes
    nsv5200303copy number variation1nstd102humanPathogenic GRCh37 chr1: 145,818,702-149,378,266 , GRCh38.p12 chr7: 58,093,723-62,429,627 , GRCh38.p12 chr1: 144,536,526-148,549,211 , LOC105371254, 151 more genes
    nsv5074192mobile element insertion1nstd203human GRCh38 chr1: 145,843,497-145,843,506 , GRCh37.p13 chr1|NW_003871055.3: 2,658,910-2,658,919 , GRCh37.p13 chr1: 145,591,562-145,591,571 POLR3C, NUDT17
    nsv5068483mobile element insertion1nstd203human GRCh38 chr1: 145,843,496-145,843,506 , GRCh37.p13 chr1|NW_003871055.3: 2,658,909-2,658,919 , GRCh37.p13 chr1: 145,591,562-145,591,572 NUDT17, POLR3C
    nsv5060379mobile element insertion1nstd203human GRCh38 chr1: 145,843,491-145,843,506 , GRCh37.p13 chr1|NW_003871055.3: 2,658,904-2,658,919 , GRCh37.p13 chr1: 145,591,562-145,591,577 POLR3C, NUDT17
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