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Items: 1 to 20 of 202

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7052713inversion1nstd229human GRCh38 chr3: 157,597,797-157,601,164 , GRCh37.p13 chr3: 157,315,586-157,318,953 SLC66A1L
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7043781inversion1nstd229human GRCh38 chr3: 157,475,033-157,814,751 , GRCh37.p13 chr3: 157,192,822-157,532,540 SLC66A1L, VEPH1
    nsv6737805copy number variation1nstd229human GRCh38 chr3: 157,582,514-157,587,628 , GRCh37.p13 chr3: 157,300,303-157,305,417 SLC66A1L
    nsv6731234copy number variation1nstd229human GRCh38 chr3: 157,586,937-158,968,270 , GRCh37.p13 chr3: 157,304,726-158,686,059 LOC100287290, LILRA2P1, 17 more genes
    nsv6730441copy number variation1nstd229human GRCh38 chr3: 157,447,224-157,552,084 , GRCh37.p13 chr3: 157,165,013-157,269,873 VEPH1, SLC66A1L
    nsv6729021copy number variation1nstd229human GRCh38 chr3: 157,553,726-157,619,179 , GRCh37.p13 chr3: 157,271,515-157,336,968 SLC66A1L
    nsv6725015copy number variation1nstd229human GRCh38 chr3: 157,540,079-157,546,107 , GRCh37.p13 chr3: 157,257,868-157,263,896 SLC66A1L
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6568046inversion1nstd223human GRCh38 chr3: 157,595,985-157,596,923 , GRCh37.p13 chr3: 157,313,774-157,314,712 SLC66A1L
    nsv6374503copy number variation1nstd223human GRCh38 chr3: 157,555,301-157,559,600 , GRCh37.p13 chr3: 157,273,090-157,277,389 SLC66A1L
    nsv6373247copy number variation1nstd223human GRCh38 chr3: 157,549,824-157,550,350 , GRCh37.p13 chr3: 157,267,613-157,268,139 SLC66A1L
    nsv6365178copy number variation1nstd223human GRCh38 chr3: 157,556,601-157,559,500 , GRCh37.p13 chr3: 157,274,390-157,277,289 SLC66A1L
    nsv6364971copy number variation1nstd223human GRCh38 chr3: 157,587,101-157,589,000 , GRCh37.p13 chr3: 157,304,890-157,306,789 SLC66A1L
    nsv6358049copy number variation1nstd223human GRCh38 chr3: 157,568,462-157,569,118 , GRCh37.p13 chr3: 157,286,251-157,286,907 SLC66A1L
    nsv6357475copy number variation1nstd223human GRCh38 chr3: 157,540,075-157,546,102 , GRCh37.p13 chr3: 157,257,864-157,263,891 SLC66A1L
    nsv6356859copy number variation1nstd223human GRCh38 chr3: 157,567,301-157,567,800 , GRCh37.p13 chr3: 157,285,090-157,285,589 SLC66A1L
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6313664copy number variation1nstd102humanUncertain significance GRCh37 chr3: 156,768,935-160,158,553 , GRCh38.p12 chr3: 157,051,146-160,440,765 LOC105374179, RPL15P6, 49 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
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