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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148201copy number variation1nstd102humanPathogenic GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857 NECTIN3, H2BP3, 418 more genes
    nsv7096531copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,489,192-125,313,644 , GRCh38.p12 chr3: 121,770,345-125,594,800 MEMO1P6, HACD2, 62 more genes
    nsv7051864inversion1nstd229human GRCh38 chr3: 121,708,189-122,055,779 , GRCh37.p13 chr3: 121,427,036-121,774,626 GOLGB1, LOC101927010, 5 more genes
    nsv7046540inversion1nstd229human GRCh38 chr3: 121,879,351-122,055,789 , GRCh37.p13 chr3: 121,598,198-121,774,636 LOC101927010, CD86, 3 more genes
    nsv6715495copy number variation1nstd229human GRCh38 chr3: 121,926,780-121,929,139 , GRCh37.p13 chr3: 121,645,627-121,647,986 SLC15A2
    nsv6714687copy number variation1nstd229human GRCh38 chr3: 121,899,101-121,910,600 , GRCh37.p13 chr3: 121,617,948-121,629,447 SLC15A2
    nsv6714601copy number variation1nstd229human GRCh38 chr3: 121,939,593-121,942,598 , GRCh37.p13 chr3: 121,658,440-121,661,445 SLC15A2
    nsv6711701copy number variation1nstd229human GRCh38 chr3: 121,894,202-121,908,545 , GRCh37.p13 chr3: 121,613,049-121,627,392 SLC15A2
    nsv6710163copy number variation1nstd229human GRCh38 chr3: 121,896,720-121,900,219 , GRCh37.p13 chr3: 121,615,567-121,619,066 SLC15A2
    nsv6707907copy number variation1nstd229human GRCh38 chr3: 113,856,250-122,791,940 , GRCh37.p13 chr3: 113,575,097-122,510,787 COX17, LOC105374052, 133 more genes
    nsv6703931copy number variation1nstd229human GRCh38 chr3: 118,573,267-126,079,281 , GRCh37.p13 chr3: 118,292,114-125,798,124 RPS24P9, LOC105374064, 149 more genes
    nsv6700911copy number variation1nstd229human GRCh38 chr3: 121,913,130-121,916,015 , GRCh37.p13 chr3: 121,631,977-121,634,862 SLC15A2
    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
    nsv6637139copy number variation1nstd102humanUncertain significance GRCh37 chr3: 121,661,753-121,767,890 , GRCh38.p12 chr3: 121,942,906-122,049,043 SLC15A2, ILDR1, 1 more genes
    nsv6566042inversion1nstd223human GRCh38 chr3: 121,928,473-121,928,706 , GRCh37.p13 chr3: 121,647,320-121,647,553 SLC15A2
    nsv6559999inversion1nstd223human GRCh38 chr3: 121,928,915-121,929,032 , GRCh37.p13 chr3: 121,647,762-121,647,879 SLC15A2
    nsv6372903copy number variation1nstd223human GRCh38 chr3: 121,922,572-121,942,534 , GRCh37.p13 chr3: 121,641,419-121,661,381 SLC15A2
    nsv6361564copy number variation1nstd223human GRCh38 chr3: 121,898,501-121,899,105 , GRCh37.p13 chr3: 121,617,348-121,617,952 SLC15A2
    nsv6361341copy number variation1nstd223human GRCh38 chr3: 121,921,379-121,921,756 , GRCh37.p13 chr3: 121,640,226-121,640,603 SLC15A2
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
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