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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094005copy number variation1nstd102humanUncertain significance GRCh37 chr13: 93,879,710-96,443,284 , GRCh38.p12 chr13: 93,227,457-95,791,030 RNA5SP36, HNRNPA1P29, 33 more genes
    nsv6952019copy number variation1nstd229human GRCh38 chr13: 94,706,750-94,707,115 , GRCh37.p13 chr13: 95,359,004-95,359,369 LINC00391
    nsv6949046copy number variation1nstd229human GRCh38 chr13: 94,549,798-94,751,655 , GRCh37.p13 chr13: 95,202,052-95,403,909 RN7SL585P, GPR180, 9 more genes
    nsv6947602copy number variation1nstd229human GRCh38 chr13: 94,664,701-94,708,800 , GRCh37.p13 chr13: 95,316,955-95,361,054 LINC00391, SOX21, 1 more genes
    nsv6939492copy number variation1nstd229human GRCh38 chr13: 94,317,586-95,198,823 , GRCh37.p13 chr13: 94,969,840-95,851,077 TRF-GAA1-5, DCT, 16 more genes
    nsv6638047copy number variation1nstd102humanPathogenic GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258 CUL4A, LOC105370373, 488 more genes
    nsv6637615copy number variation1nstd102humanPathogenic GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878 SNORD13G, FTLP8, 162 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6315552copy number variation1nstd102humanPathogenic GRCh37 chr13: 89,490,345-115,062,235 , GRCh38.p12 chr13: 88,838,091-114,296,760 MIR20A, MIR548AR, 347 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314171copy number variation1nstd102humanPathogenic GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258 MIR4705, LOC102724149, 430 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6313971copy number variation1nstd102humanPathogenic GRCh37 chr13: 85,037,147-115,107,733 , GRCh38.p12 chr13: 84,463,012-114,342,258 BRK1P2, UGGT2, 386 more genes
    nsv6313904copy number variation1nstd102humanPathogenic GRCh37 chr13: 78,514,567-115,107,733 , GRCh38.p12 chr13: 77,940,432-114,342,258 LOC101927284, LOC105370330, 444 more genes
    nsv6309343copy number variation1nstd102humanUncertain significance GRCh37 chr13: 95,034,648-96,443,284 , GRCh38.p12 chr13: 94,382,394-95,791,030 CLDN10, RPL21P112, 29 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6133114copy number variation1nstd213human GRCh37 chr13: 95,330,000-95,480,001 , GRCh38.p12 chr13: 94,677,746-94,827,747 SOX21, BRD7P5, 6 more genes
    nsv6133110copy number variation1nstd213human GRCh37 chr13: 86,910,000-96,620,001 , GRCh38.p12 chr13: 86,292,878-95,967,747 DCT, GPC5, 102 more genes
    nsv6132849copy number variation1nstd213human GRCh37 chr13: 87,820,000-112,350,001 , GRCh38.p12 chr13: 87,167,745-111,697,654 PARP1P1, COL4A1, 301 more genes
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