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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097266copy number variation1nstd102humanPathogenic GRCh37 chr5: 167,849,013-169,661,202 , GRCh38.p12 chr5: 168,422,008-170,234,198 FBLL1, RNU6-477P, 25 more genes
    nsv7048806inversion1nstd229human GRCh38 chr5: 168,414,285-168,784,754 , GRCh37.p13 chr5: 167,841,290-168,211,759 FBLL1, MIR103A1, 9 more genes
    nsv7042332inversion1nstd229human GRCh38 chr5: 168,444,570-168,573,004 , GRCh37.p13 chr5: 167,871,575-168,000,009 WWC1, FBLL1, 5 more genes
    nsv6796477copy number variation1nstd229human GRCh38 chr5: 168,531,878-169,361,925 , GRCh37.p13 chr5: 167,958,883-168,788,929 MIR103A1, MIR218-2, 11 more genes
    nsv6783543copy number variation1nstd229human GRCh38 chr5: 168,394,301-168,784,700 , GRCh37.p13 chr5: 167,821,306-168,211,705 RPL10P9, WWC1, 9 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6136094copy number variation1nstd213human GRCh37 chr5: 167,490,000-168,160,001 , GRCh38.p12 chr5: 168,062,995-168,732,996 RARS1, SLIT3, 11 more genes
    nsv6136093copy number variation1nstd213human GRCh37 chr5: 166,260,000-169,230,001 , GRCh38.p12 chr5: 166,832,995-169,802,997 DOCK2, RARS1, 26 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv4729368copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 166,378,793-170,174,830 , GRCh38.p12 chr5: 166,951,788-170,747,826 DOCK2, FOXI1, 38 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4455586copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349 LOC105377677, GABRA6, 164 more genes
    nsv4318527inversion1nstd166human GRCh37.p13 chr5: 166,866,478-168,367,440 , GRCh38.p12 chr5: 167,439,473-168,940,435 , RARS1, 16 more genes
    nsv3924400copy number variation1nstd102humanPathogenic NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805 CEP192P1, ARL2BPP6, 443 more genes
    nsv3921186copy number variation1nstd102humanPathogenic GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412 TENM2, LOC107986479, 347 more genes
    nsv3921182copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758 RN7SKP148, TCOF1, 553 more genes
    nsv3920339copy number variation1nstd102humanPathogenic NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805 MIR1229, LOC105377713, 343 more genes
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