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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901718copy number variation1nstd209human GRCh38 chr5: 172,153,284-177,326,767 , GRCh37.p13 chr5: 171,580,288-176,753,768 , LOC107986487, 114 more genes
    nsv5897737copy number variation1nstd209human GRCh38 chr5: 173,697,434-173,697,491 , GRCh37.p13 chr5: 173,124,437-173,124,494 LINC01942
    nsv5466768copy number variation1nstd206human GRCh38 chr5: 173,690,183-173,690,240 , GRCh37.p13 chr5: 173,117,186-173,117,243 LINC01942
    nsv5457601copy number variation1nstd206human GRCh38 chr5: 173,697,434-173,697,493 , GRCh37.p13 chr5: 173,124,437-173,124,496 LINC01942
    nsv4949231copy number variation1nstd200human GRCh38 chr5: 173,571,609-173,858,663 , GRCh37.p13 chr5: 172,998,612-173,285,666 , BOD1, 7 more genes
    nsv4768375copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,805,664-180,719,789 , GRCh38.p12 chr5: 171,378,660-181,292,788 LINC01863, PRDX2P3, 279 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4742704copy number variation1nstd199human GRCh37 chr5: 173,126,673-173,126,863 , GRCh38.p12 chr5: 173,699,670-173,699,860 LINC01942
    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
    nsv4386404copy number variation1nstd173human GRCh37 chr5: 173,003,224-173,280,734 , GRCh38.p12 chr5: 173,576,221-173,853,731 , LINC02995, 7 more genes
    nsv4312190insertion1nstd166human GRCh37.p13 chr5: 173,130,684-173,130,684 , GRCh38.p12 chr5: 173,703,681-173,703,681 LINC01942
    nsv3956819copy number variation1nstd168human GRCh38 chr5: 173,578,864-173,817,726 , GRCh37.p13 chr5: 173,005,867-173,244,729 , BOD1, 7 more genes
    nsv3924705copy number variation1nstd102humanPathogenic GRCh38 chr5: 173,237,772-176,614,618 , GRCh37 chr5: 172,664,775-176,041,619 , NCBI36 chr5: 172,597,381-175,974,225 RNF44, OR1X1P, 62 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
    nsv3919616copy number variation1nstd102humanPathogenic GRCh37 chr5: 172,203,801-173,769,972 , GRCh38 chr5: 172,776,798-174,342,969 , NCBI36 chr5: 172,136,407-173,702,578 LINC02995, CPEB4, 33 more genes
    nsv3918887copy number variation1nstd102humanPathogenic GRCh37 chr5: 168,761,759-180,712,302 , NCBI36 chr5: 168,694,337-180,644,908 , GRCh38 chr5: 169,334,755-181,285,301 RPS8P7, LOC107986476, 311 more genes
    nsv3914710copy number variation1nstd102humanPathogenic GRCh38 chr5: 172,961,091-175,054,665 , GRCh37 chr5: 172,388,094-174,481,668 , NCBI36 chr5: 172,320,700-174,414,274 NKX2-5, CDC42P5, 40 more genes
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