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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5889988copy number variation1nstd209human GRCh38 chr4: 52,051,821-52,051,904 , GRCh37.p13 chr4: 52,917,987-52,918,070 SPATA18
    nsv5675000mobile element insertion1nstd211human GRCh38 chr4: 52,064,472-52,064,472 , GRCh37.p13 chr4: 52,930,638-52,930,638 SPATA18
    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
    nsv5608645insertion1nstd207human GRCh38 chr4: 52,081,945-52,081,945 , GRCh37.p13 chr4: 52,948,111-52,948,111 SPATA18
    nsv5566861copy number variation1nstd207human GRCh38 chr4: 52,051,821-52,051,904 , GRCh37.p13 chr4: 52,917,987-52,918,070 SPATA18
    nsv5547415insertion1nstd206human GRCh38 chr4: 52,072,249-52,072,300 , GRCh37.p13 chr4: 52,938,415-52,938,466 SPATA18
    nsv5472805copy number variation1nstd206human GRCh38 chr4: 52,051,823-52,051,905 , GRCh37.p13 chr4: 52,917,989-52,918,071 SPATA18
    nsv5466445copy number variation1nstd206human GRCh38 chr4: 52,081,945-52,082,092 , GRCh37.p13 chr4: 52,948,111-52,948,258 SPATA18
    nsv5462241copy number variation1nstd206human GRCh38 chr4: 52,070,275-52,070,518 , GRCh37.p13 chr4: 52,936,441-52,936,684 SPATA18
    nsv5388271copy number variation3nstd186human GRCh37 chr4: 52,948,111-52,948,258 , GRCh38.p12 chr4: 52,081,945-52,082,092 SPATA18
    nsv5352926translocation1nstd200human GRCh38 chr4: 52,051,905-52,051,905 , GRCh38 chr4: 52,051,823-52,051,823 , GRCh37.p13 chr4: 52,918,071-52,918,071 , GRCh37.p13 chr4: 52,917,989-52,917,989 SPATA18
    nsv5171440mobile element insertion1nstd203human GRCh38 chr4: 52,061,659-52,061,668 , GRCh37.p13 chr4: 52,927,825-52,927,834 SPATA18
    nsv5164864mobile element insertion1nstd203human GRCh38 chr4: 52,061,654-52,061,668 , GRCh37.p13 chr4: 52,927,820-52,927,834 SPATA18
    nsv5090797mobile element insertion1nstd203human GRCh38 chr4: 52,064,460-52,064,472 , GRCh37.p13 chr4: 52,930,626-52,930,638 SPATA18
    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
    nsv4925604copy number variation1nstd200human GRCh38 chr4: 52,081,945-52,082,092 , GRCh37.p13 chr4: 52,948,111-52,948,258 SPATA18
    nsv4913259copy number variation1nstd200human GRCh38 chr4: 52,077,479-52,078,874 , GRCh37.p13 chr4: 52,943,645-52,945,040 SPATA18
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4809225copy number variation1nstd200human GRCh37 chr4: 52,948,111-52,948,258 , GRCh38.p12 chr4: 52,081,945-52,082,092 SPATA18
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