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Items: 1 to 20 of 647

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146974insertion1nstd232human GRCh37.p13 chr22: 45,300,386-45,300,386 , GRCh38.p12 chr22: 44,904,506-44,904,506 PHF21B
    nsv7139779insertion1nstd232human GRCh37.p13 chr22: 45,340,790-45,340,790 , GRCh38.p12 chr22: 44,944,910-44,944,910 PHF21B
    nsv7098949copy number variation1nstd102humanUncertain significance GRCh38 chr22: 44,184,196-45,239,435 , GRCh37.p13 chr22: 44,580,076-45,635,316 PARVG, RTL6, 22 more genes
    nsv7076597inversion1nstd229human GRCh38 chr22: 44,931,200-44,945,973 , GRCh37.p13 chr22: 45,327,080-45,341,853 PHF21B
    nsv7075301inversion1nstd229human GRCh38 chr22: 44,922,920-44,923,022 , GRCh37.p13 chr22: 45,318,800-45,318,902 PHF21B
    nsv7074464inversion1nstd229human GRCh38 chr22: 43,918,591-49,788,574 , GRCh37.p13 chr22: 44,314,471-50,182,222 LOC107985536, LINC02939, 94 more genes
    nsv7073216inversion1nstd229human GRCh38 chr22: 44,951,540-44,952,816 , GRCh37.p13 chr22: 45,347,420-45,348,696 PHF21B
    nsv7072712inversion1nstd229human GRCh38 chr22: 44,866,018-44,928,522 , GRCh37.p13 chr22: 45,261,898-45,324,402 PHF21B, RPL6P28
    nsv7064353inversion1nstd229human GRCh38 chr22: 44,878,322-44,879,580 , GRCh37.p13 chr22: 45,274,202-45,275,460 PHF21B
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7037689copy number variation1nstd229human GRCh38 chr22: 44,973,673-44,973,706 , GRCh37.p13 chr22: 45,369,553-45,369,586 PHF21B
    nsv7036493copy number variation1nstd229human GRCh38 chr22: 44,971,319-44,972,991 , GRCh37.p13 chr22: 45,367,199-45,368,871 PHF21B
    nsv7035576copy number variation1nstd229human GRCh38 chr22: 44,917,997-44,919,900 , GRCh37.p13 chr22: 45,313,877-45,315,780 PHF21B
    nsv7034862copy number variation1nstd229human GRCh38 chr22: 44,940,394-44,954,165 , GRCh37.p13 chr22: 45,336,274-45,350,045 PHF21B
    nsv7034514copy number variation1nstd229human GRCh38 chr22: 44,861,260-44,879,807 , GRCh37.p13 chr22: 45,257,140-45,275,687 PRR5-ARHGAP8, ARHGAP8, 2 more genes
    nsv7033895copy number variation1nstd229human GRCh38 chr22: 44,928,201-44,948,600 , GRCh37.p13 chr22: 45,324,081-45,344,480 PHF21B
    nsv7033609copy number variation1nstd229human GRCh38 chr22: 44,978,301-44,993,500 , GRCh37.p13 chr22: 45,374,181-45,389,380 PHF21B
    nsv7033505copy number variation1nstd229human GRCh38 chr22: 44,958,070-44,961,671 , GRCh37.p13 chr22: 45,353,950-45,357,551 PHF21B
    nsv7033360copy number variation1nstd229human GRCh38 chr22: 44,956,617-44,956,639 , GRCh37.p13 chr22: 45,352,497-45,352,519 PHF21B
    nsv7033254copy number variation1nstd229human GRCh38 chr22: 44,977,376-44,983,433 , GRCh37.p13 chr22: 45,373,256-45,379,313 PHF21B
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