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Items: 1 to 20 of 103

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6737279copy number variation1nstd229human GRCh38 chr4: 52,859,601-52,873,800 , GRCh37.p13 chr4: 53,725,768-53,739,967 SCFD2, RASL11B
    nsv6734289copy number variation1nstd229human GRCh38 chr4: 52,859,715-52,870,406 , GRCh37.p13 chr4: 53,725,882-53,736,573 RASL11B
    nsv6723716copy number variation1nstd229human GRCh38 chr4: 52,741,446-52,878,111 , GRCh37.p13 chr4: 53,607,613-53,744,278 RASL11B, LINC01618, 3 more genes
    nsv6721972copy number variation1nstd229human GRCh38 chr4: 52,833,647-52,863,790 , GRCh37.p13 chr4: 53,699,814-53,729,957 RASL11B
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6637004copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,098,544-53,949,065 , GRCh38.p12 chr4: 52,232,378-53,082,898 LINC01618, LOC107986279, 12 more genes
    nsv6636907copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,434,611-54,079,547 , GRCh38.p12 chr4: 52,568,445-53,213,380 USP46, LOC107986281, 9 more genes
    nsv6636355copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,715,514-53,925,549 , GRCh38.p12 chr4: 52,849,347-53,059,382 SCFD2, RASL11B, 1 more genes
    nsv6315421copy number variation1nstd102humanPathogenic GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280 METTL5P3, RPL38P3, 38 more genes
    nsv6313624copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,091,609-53,953,124 , GRCh38.p12 chr4: 52,225,443-53,086,957 LOC100419861, RASL11B, 12 more genes
    nsv6313491copy number variation1nstd102humanUncertain significance GRCh37 chr4: 53,435,144-54,091,178 , GRCh38.p12 chr4: 52,568,978-53,225,011 USP46-DT, RASL11B, 9 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5460262copy number variation1nstd206human GRCh38 chr4: 52,853,615-52,866,907 , GRCh37.p13 chr4: 53,719,782-53,733,074 RASL11B
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
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