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Items: 1 to 20 of 467

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098826copy number variation1nstd102humanLikely pathogenic GRCh38 chr2: 31,621,429-31,624,204 , GRCh37.p13 chr2: 31,846,498-31,849,273 SRD5A2
    nsv7096499copy number variation2nstd102humanUncertain significance GRCh37 chr2: 31,598,226-31,805,969 , GRCh38.p12 chr2: 31,375,360-31,580,900 SRD5A2, XDH
    nsv7050455inversion1nstd229human GRCh38 chr2: 31,632,871-31,651,208 , GRCh37.p13 chr2: 31,857,940-31,876,277 SRD5A2
    nsv7047639inversion1nstd229human GRCh38 chr2: 29,857,017-35,800,286 , GRCh37.p13 chr2: 30,079,883-36,025,352 LTBP1, KRT18P52, 67 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv6677185copy number variation1nstd229human GRCh38 chr2: 31,645,349-31,726,221 , GRCh37.p13 chr2: 31,870,418-31,951,290 SRD5A2, LOC107985862
    nsv6676777copy number variation1nstd229human GRCh38 chr2: 31,618,101-31,651,400 , GRCh37.p13 chr2: 31,843,170-31,876,469 SRD5A2
    nsv6675811copy number variation1nstd229human GRCh38 chr2: 31,541,748-31,548,047 , GRCh37.p13 chr2: 31,766,818-31,773,117 SRD5A2
    nsv6673704copy number variation1nstd229human GRCh38 chr2: 31,558,654-31,561,119 , GRCh37.p13 chr2: 31,783,724-31,786,189 SRD5A2
    nsv6672958copy number variation1nstd229human GRCh38 chr2: 31,596,705-31,600,689 , GRCh37.p13 chr2: 31,821,774-31,825,758 SRD5A2
    nsv6672937copy number variation1nstd229human GRCh38 chr2: 31,643,572-31,646,168 , GRCh37.p13 chr2: 31,868,641-31,871,237 SRD5A2
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6672633copy number variation1nstd229human GRCh38 chr2: 31,605,601-31,609,600 , GRCh37.p13 chr2: 31,830,670-31,834,669 SRD5A2
    nsv6672155copy number variation1nstd229human GRCh38 chr2: 31,580,457-31,580,516 , GRCh37.p13 chr2: 31,805,527-31,805,586 SRD5A2
    nsv6671317copy number variation1nstd229human GRCh38 chr2: 31,554,514-31,561,119 , GRCh37.p13 chr2: 31,779,584-31,786,189 SRD5A2
    nsv6670698copy number variation1nstd229human GRCh38 chr2: 31,375,332-31,644,278 , GRCh37.p13 chr2: 31,598,198-31,869,347 SRD5A2, XDH
    nsv6670154copy number variation1nstd229human GRCh38 chr2: 31,665,668-31,699,086 , GRCh37.p13 chr2: 31,890,737-31,924,155 SRD5A2, LOC107985862
    nsv6670009copy number variation1nstd229human GRCh38 chr2: 31,568,432-31,572,300 , GRCh37.p13 chr2: 31,793,502-31,797,370 SRD5A2
    nsv6669465copy number variation1nstd229human GRCh38 chr2: 31,663,701-31,769,900 , GRCh37.p13 chr2: 31,888,770-31,994,969 LOC107985862, LOC107985863, 1 more genes
    nsv6669082copy number variation1nstd229human GRCh38 chr2: 31,625,849-31,627,751 , GRCh37.p13 chr2: 31,850,918-31,852,820 SRD5A2
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