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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6792791copy number variation1nstd229human GRCh38 chr5: 171,786,284-171,786,674 , GRCh37.p13 chr5: 171,213,288-171,213,678 SMIM23
    nsv6781511copy number variation1nstd229human GRCh38 chr5: 170,662,244-174,111,903 , GRCh37.p13 chr5: 170,089,248-173,538,906 LOC101928093, LOC107986482, 79 more genes
    nsv6780650copy number variation1nstd229human GRCh38 chr5: 171,733,101-171,829,600 , GRCh37.p13 chr5: 171,160,105-171,256,604 LOC105377724, LOC105377725, 2 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
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 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
    nsv6281526insertion1nstd214human GRCh38 chr5: 171,782,876-171,782,876 , GRCh37.p13 chr5: 171,209,880-171,209,880 SMIM23
    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
    nsv5720711mobile element insertion1nstd211human GRCh38 chr5: 171,789,647-171,789,647 , GRCh37.p13 chr5: 171,216,651-171,216,651 SMIM23
    nsv5467796copy number variation1nstd206human GRCh38 chr5: 171,782,876-171,782,963 , GRCh37.p13 chr5: 171,209,880-171,209,967 SMIM23
    nsv5362696translocation1nstd200human GRCh38 chr5: 171,775,477-171,775,477 , GRCh38 chr5: 171,775,579-171,775,579 , GRCh37.p13 chr5: 171,202,481-171,202,481 , GRCh37.p13 chr5: 171,202,583-171,202,583 SMIM23
    nsv4815498copy number variation1nstd200human GRCh37 chr5: 171,202,481-171,202,583 , GRCh38.p12 chr5: 171,775,477-171,775,579 SMIM23
    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
    nsv4456265copy number variation1nstd102humanUncertain significance GRCh37 chr5: 171,171,671-172,022,583 , GRCh38.p12 chr5: 171,744,667-172,595,580 STK10, SH3PXD2B, 11 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
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