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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138538insertion1nstd232human GRCh37.p13 chr3: 124,641,547-124,641,547 , GRCh38.p12 chr3: 124,922,700-124,922,700 MUC13
    nsv7096928copy number variation1nstd102humanUncertain significance GRCh37 chr3: 123,003,455-125,313,644 , GRCh38.p12 chr3: 123,284,608-125,594,800 MIR544B, OSBPL11, 33 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
    nsv7053781inversion1nstd229human GRCh38 chr3: 123,490,767-125,244,776 , GRCh37.p13 chr3: 123,209,614-124,963,620 MIR6083, MYLK, 25 more genes
    nsv6716976copy number variation1nstd229human GRCh38 chr3: 124,912,715-124,913,817 , GRCh37.p13 chr3: 124,631,562-124,632,664 MUC13
    nsv6716447copy number variation1nstd229human GRCh38 chr3: 124,931,894-124,932,282 , GRCh37.p13 chr3: 124,650,738-124,651,126 MUC13
    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
    nsv6703605copy number variation1nstd229human GRCh38 chr3: 124,911,368-124,950,452 , GRCh37.p13 chr3: 124,630,215-124,669,296 MUC13
    nsv6699037copy number variation1nstd229human GRCh38 chr3: 124,629,401-124,952,500 , GRCh37.p13 chr3: 124,348,248-124,671,344 MUC13, ITGB5, 5 more genes
    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
    nsv6562259inversion1nstd223human GRCh38 chr3: 123,977,549-125,974,993 , GRCh37.p13 chr3: 123,696,396-125,693,836 ROPN1B, DNAJB6P7, 46 more genes
    nsv6556022inversion1nstd223human GRCh38 chr3: 123,151,729-129,172,574 , GRCh37.p13 chr3: 122,870,576-128,891,417 UMPS, CHST13, 139 more genes
    nsv6370714copy number variation1nstd223human GRCh38 chr3: 124,914,279-124,915,576 , GRCh37.p13 chr3: 124,633,126-124,634,423 MUC13
    nsv6370243copy number variation1nstd223human GRCh38 chr3: 124,931,772-124,932,293 , GRCh37.p13 chr3: 124,650,616-124,651,137 MUC13
    nsv6368075copy number variation1nstd223human GRCh38 chr3: 124,929,396-124,929,736 , GRCh37.p13 chr3: 124,648,240-124,648,580 MUC13
    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
    nsv6296531copy number variation1nstd186human GRCh37 chr3: 124,650,629-124,651,137 , GRCh38.p12 chr3: 124,931,785-124,932,293 MUC13
    nsv6283416insertion1nstd214human GRCh38 chr3: 124,920,553-124,920,553 , GRCh37.p13 chr3: 124,639,400-124,639,400 MUC13
    nsv6262512copy number variation1nstd214human GRCh38 chr3: 124,904,109-124,904,171 , GRCh37.p13 chr3: 124,622,956-124,623,018 MUC13
    nsv6225045insertion2nstd214human GRCh38 chr3: 124,922,700-124,922,700 , GRCh37.p13 chr3: 124,641,547-124,641,547 MUC13
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