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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6644544copy number variation1nstd229human GRCh38 chr1: 170,153,701-170,159,000 , GRCh37.p13 chr1: 170,122,842-170,128,141 NTMT2
    nsv6644498copy number variation1nstd229human GRCh38 chr1: 170,154,601-170,158,800 , GRCh37.p13 chr1: 170,123,742-170,127,941 NTMT2
    nsv6644494copy number variation1nstd229human GRCh38 chr1: 170,089,146-170,255,367 , GRCh37.p13 chr1: 170,058,287-170,224,508 SIGLEC30P, MIR3119-1, 4 more genes
    nsv6644490copy number variation1nstd229human GRCh38 chr1: 169,979,861-170,252,213 , GRCh37.p13 chr1: 169,949,002-170,221,354 MRPS10P1, KIFAP3, 6 more genes
    nsv6644429copy number variation1nstd229human GRCh38 chr1: 170,145,288-170,145,637 , GRCh37.p13 chr1: 170,114,429-170,114,778 NTMT2
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6644049copy number variation1nstd229human GRCh38 chr1: 170,169,301-170,181,500 , GRCh37.p13 chr1: 170,138,442-170,150,641 NTMT2, LINC01681
    nsv6644048copy number variation1nstd229human GRCh38 chr1: 170,154,656-170,159,128 , GRCh37.p13 chr1: 170,123,797-170,128,269 NTMT2
    nsv6644047copy number variation1nstd229human GRCh38 chr1: 170,154,501-170,159,100 , GRCh37.p13 chr1: 170,123,642-170,128,241 NTMT2
    nsv6625875copy number variation1nstd224human GRCh37 chr1: 169,547,458-170,642,899 , GRCh38.p12 chr1: 169,578,220-170,673,758 SELP, GORAB, 23 more genes
    nsv6625672copy number variation1nstd224human GRCh37 chr1: 170,065,845-170,505,585 , GRCh38.p12 chr1: 170,096,704-170,536,444 GORAB, HAUS4P1, 8 more genes
    nsv6335059copy number variation1nstd223human GRCh38 chr1: 170,156,665-170,157,092 , GRCh37.p13 chr1: 170,125,806-170,126,233 NTMT2
    nsv6334649copy number variation1nstd223human GRCh38 chr1: 170,157,401-170,158,900 , GRCh37.p13 chr1: 170,126,542-170,128,041 NTMT2
    nsv6333648copy number variation1nstd223human GRCh38 chr1: 170,089,146-170,255,361 , GRCh37.p13 chr1: 170,058,287-170,224,502 SIGLEC30P, NTMT2, 4 more genes
    nsv6318737copy number variation1nstd223human GRCh38 chr1: 170,154,656-170,159,124 , GRCh37.p13 chr1: 170,123,797-170,128,265 NTMT2
    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
    nsv6310918copy number variation1nstd102humanPathogenic GRCh37 chr1: 169,660,781-170,521,603 , GRCh38.p12 chr1: 169,691,640-170,552,462 GORAB-AS1, RN7SL333P, 18 more genes
    nsv6290484copy number variation1nstd102humanLikely benign GRCh37 chr1: 170,057,514-170,223,438 , GRCh38.p12 chr1: 170,088,373-170,254,297 SIGLEC30P, NTMT2, 4 more genes
    nsv6133938copy number variation1nstd213human GRCh37 chr1: 169,800,000-170,240,001 , GRCh38.p12 chr1: 169,830,859-170,270,860 KIFAP3, FIRRM, 11 more genes
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