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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
    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
    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
    nsv4456020copy number variation1nstd102humanUncertain significance GRCh37 chr5: 172,657,979-172,782,386 , GRCh38.p12 chr5: 173,230,976-173,355,383 NKX2-5, LOC105377731, 4 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
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3885523copy number variation1nstd102humanPathogenic GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343 WWC1, CNOT6, 446 more genes
    nsv3884275copy number variation1nstd102humanLikely benign GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409 LOC107986368, PRELID3BP9, 1258 more genes
    nsv3879307copy number variation1nstd102humanPathogenic GRCh37 chr5: 164,207,156-172,799,124 , GRCh38.p12 chr5: 164,780,150-173,372,121 RN7SL339P, LOC107986472, 113 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
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