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Items: 1 to 20 of 87

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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
    nsv6794412copy number variation1nstd229human GRCh38 chr5: 171,566,701-171,598,100 , GRCh37.p13 chr5: 170,993,705-171,025,104 LOC107986392, LOC105377722
    nsv6785752copy number variation1nstd229human GRCh38 chr5: 171,578,435-171,579,204 , GRCh37.p13 chr5: 171,005,439-171,006,208 LOC107986392, LOC105377722
    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
    nsv6781433copy number variation1nstd229human GRCh38 chr5: 171,452,630-171,585,751 , GRCh37.p13 chr5: 170,879,634-171,012,755 FGF18, LOC105377721, 3 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
    nsv6295736copy number variation1nstd186human GRCh37 chr5: 171,004,044-171,005,326 , GRCh38.p12 chr5: 171,577,040-171,578,322 LOC105377722, LOC107986392
    nsv6289957copy number variation1nstd102humanUncertain significance GRCh37 chr5: 170,814,836-171,100,000 , GRCh38.p12 chr5: 171,387,832-171,672,996 LOC107986392, LOC105377722, 4 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
    nsv5454219copy number variation1nstd206human GRCh38 chr5: 171,577,040-171,578,322 , GRCh37.p13 chr5: 171,004,044-171,005,326 LOC105377722, LOC107986392
    nsv4939907copy number variation1nstd200human GRCh38 chr5: 171,573,288-171,573,386 , GRCh37.p13 chr5: 171,000,292-171,000,390 LOC107986392, LOC105377722
    nsv4815491copy number variation1nstd200human GRCh37 chr5: 171,000,292-171,000,390 , GRCh38.p12 chr5: 171,573,288-171,573,386 LOC107986392, LOC105377722
    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
    nsv4481665mobile element insertion1nstd166human GRCh37.p13 chr5: 171,007,550-171,007,550 , GRCh38.p12 chr5: 171,580,546-171,580,546 LOC105377722, LOC107986392
    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
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