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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6795187copy number variation1nstd229human GRCh38 chr5: 171,283,101-171,715,500 , GRCh37.p13 chr5: 170,710,105-171,142,504 RPL19P10, RANBP17, 12 more genes
    nsv6791548copy number variation1nstd229human GRCh38 chr5: 170,914,278-171,309,894 , GRCh37.p13 chr5: 170,341,282-170,736,898 TLX3, USP12P1, 1 more genes
    nsv6787062copy number variation1nstd229human GRCh38 chr5: 171,207,129-171,524,655 , GRCh37.p13 chr5: 170,634,133-170,951,659 RPL10P8, FGF18, 11 more genes
    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
    nsv6779337copy number variation1nstd229human GRCh38 chr5: 171,309,501-171,310,500 , GRCh37.p13 chr5: 170,736,505-170,737,504 TLX3
    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
    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
    nsv6134988copy number variation1nstd213human GRCh37 chr5: 170,720,000-170,980,001 , GRCh38.p12 chr5: 171,292,996-171,552,997 NPM1, FGF18, 10 more genes
    nsv4763538inversion1nstd199human GRCh37 chr5: 170,260,689-178,183,120 , GRCh38.p12 chr5: 170,833,685-178,756,119 , BNIP1, 194 more genes
    nsv4597888copy number variation1nstd183human GRCh37 chr5: 170,063,238-170,780,570 , GRCh38.p12 chr5: 170,636,234-171,353,566 LOC107986474, GABRP, 10 more genes
    nsv4592792copy number variation1nstd183human GRCh37 chr5: 170,063,076-170,777,960 , GRCh38.p12 chr5: 170,636,072-171,350,956 KCNIP1, LOC107986473, 10 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
    nsv4128441copy number variation1nstd166human GRCh37.p13 chr5: 170,531,533-171,085,237 , GRCh38.p12 chr5: 171,104,529-171,658,233 LOC107986392, RN7SL339P, 13 more genes
    nsv4120680copy number variation1nstd166human GRCh37.p13 chr5: 170,634,133-170,951,659 , GRCh38.p12 chr5: 171,207,129-171,524,655 RN7SL339P, TLX3, 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
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