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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3915913copy number variation1nstd102humanUncertain significance NCBI36 chr5: 167,594,245-168,386,974 , GRCh38 chr5: 168,234,662-169,027,391 , GRCh37 chr5: 167,661,667-168,454,396 MIR103A1, MIR218-2, 13 more genes
    nsv3914475copy number variation1nstd102humanUncertain significance GRCh37 chr5: 167,860,417-170,844,183 , GRCh38 chr5: 168,433,412-171,417,179 , NCBI36 chr5: 167,792,995-170,776,788 INSYN2B, LOC107986472, 48 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
    nsv3886151copy number variation1nstd102humanPathogenic GRCh37 chr5: 154,886,174-169,757,448 , GRCh38.p12 chr5: 155,506,614-170,330,444 CCNG1, LSM11, 148 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
    nsv3874238copy number variation1nstd102humanPathogenic GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337 PJA2, LOC646058, 1228 more genes
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