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Items: 1 to 20 of 220

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7054914inversion1nstd229human GRCh38 chr5: 7,255,566-7,471,609 , GRCh37.p13 chr5: 7,255,679-7,471,722 LOC107986403, LINC02142, 8 more genes
    nsv7053901inversion1nstd229human GRCh38 chr5: 3,129,013-8,027,353 , GRCh37.p13 chr5: 3,129,127-8,027,466 FASTKD3, LOC101929200, 58 more genes
    nsv7047146inversion1nstd229human GRCh38 chr5: 6,624,019-7,857,705 , GRCh37.p13 chr5: 6,624,132-7,857,818 SRD5A1, LOC105374643, 24 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv6777352copy number variation1nstd229human GRCh38 chr5: 7,120,991-7,812,776 , GRCh37.p13 chr5: 7,121,104-7,812,889 LINC02142, LOC107986403, 9 more genes
    nsv6768898copy number variation1nstd229human GRCh38 chr5: 6,859,459-8,760,979 , GRCh37.p13 chr5: 6,859,572-8,761,091 RNA5SP176, MTND6P2, 25 more genes
    nsv6762084copy number variation1nstd229human GRCh38 chr5: 6,231,049-7,367,961 , GRCh37.p13 chr5: 6,231,162-7,368,074 SRD5A1, LOC100130063, 23 more genes
    nsv6636942copy number variation1nstd102humanPathogenic GRCh37 chr5: 1-32,091,038 , GRCh38.p12 chr5: 10,001-32,090,932 LOC105374608, LSP1P3, 351 more genes
    nsv6636849copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-17,654,787 , GRCh38.p12 chr5: 113,462-17,654,678 ADCY2, HMGB3P3, 248 more genes
    nsv6636672copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-26,164,852 , GRCh38.p12 chr5: 113,462-26,164,743 LINC02123, LINC01020, 302 more genes
    nsv6636606copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,577-31,448,527 , GRCh38.p12 chr5: 113,462-31,448,420 BASP1, RNU1-76P, 338 more genes
    nsv6636345copy number variation1nstd102humanUncertain significance GRCh37 chr5: 7,073,154-7,643,024 , GRCh38.p12 chr5: 7,073,041-7,642,911 LOC105374643, LINC02123, 9 more genes
    nsv6630369copy number variation1nstd224human GRCh37 chr5: 6,804,983-7,418,630 , GRCh38.p12 chr5: 6,804,870-7,418,517 LOC100130063, RNA5SP176, 15 more genes
    nsv6574354inversion1nstd223human GRCh38 chr5: 2,721,509-7,652,209 , GRCh37.p13 chr5: 2,721,623-7,652,322 MIR4278, LOC442132, 60 more genes
    nsv6563912inversion1nstd223human GRCh38 chr5: 7,255,565-7,471,608 , GRCh37.p13 chr5: 7,255,678-7,471,721 ADCY2, LOC105374645, 8 more genes
    nsv6315441copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-29,310,520 , GRCh38.p12 chr5: 113,461-29,310,413 FBXL7, LOC105374608, 319 more genes
    nsv6315416copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-30,712,376 , GRCh38.p12 chr5: 113,461-30,712,269 LOC105374649, LINC02196, 333 more genes
    nsv6315382copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-8,007,018 , GRCh38.p12 chr5: 113,461-8,006,905 MTCO1P31, LOC100130063, 126 more genes
    nsv6315334copy number variation1nstd102humanPathogenic GRCh37 chr5: 113,576-12,601,027 , GRCh38.p12 chr5: 113,461-12,600,915 LOC105374642, LOC107986395, 173 more genes
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