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Items: 1 to 20 of 875

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7141053copy number variation1nstd232human GRCh37.p13 chr3: 10,549,594-10,549,644 , GRCh38.p12 chr3: 10,507,910-10,507,960 ATP2B2
    nsv7096923copy number variation1nstd102humanUncertain significance GRCh37 chr3: 10,400,355-10,401,827 , GRCh38.p12 chr3: 10,358,671-10,360,143 ATP2B2
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 more genes
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7053980inversion1nstd229human GRCh38 chr3: 10,492,025-10,494,797 , GRCh37.p13 chr3: 10,533,709-10,536,481 ATP2B2
    nsv7051287inversion1nstd229human GRCh38 chr3: 10,494,446-10,498,343 , GRCh37.p13 chr3: 10,536,130-10,540,027 ATP2B2
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv7041321inversion1nstd229human GRCh38 chr3: 10,273,886-10,365,534 , GRCh37.p13 chr3: 10,315,570-10,407,218 TATDN2, ATP2B2, 6 more genes
    nsv6717494copy number variation1nstd229human GRCh38 chr3: 10,553,154-10,581,324 , GRCh37.p13 chr3: 10,594,838-10,623,008 ATP2B2
    nsv6717121copy number variation1nstd229human GRCh38 chr3: 10,672,151-10,672,301 , GRCh37.p13 chr3: 10,713,836-10,713,986 ATP2B2
    nsv6717074copy number variation1nstd229human GRCh38 chr3: 10,616,700-10,642,453 , GRCh37.p13 chr3: 10,658,385-10,684,138 ATP2B2, ATP2B2-IT2
    nsv6716389copy number variation1nstd229human GRCh38 chr3: 10,589,197-10,593,739 , GRCh37.p13 chr3: 10,630,881-10,635,424 ATP2B2
    nsv6716189copy number variation1nstd229human GRCh38 chr3: 10,417,159-10,417,343 , GRCh37.p13 chr3: 10,458,843-10,459,027 ATP2B2
    nsv6715869copy number variation1nstd229human GRCh38 chr3: 9,686,801-10,627,600 , GRCh37.p13 chr3: 9,728,485-10,669,285 FANCD2OS, CRELD1, 40 more genes
    nsv6715020copy number variation1nstd229human GRCh38 chr3: 10,572,969-10,579,505 , GRCh37.p13 chr3: 10,614,653-10,621,189 ATP2B2
    nsv6714405copy number variation1nstd229human GRCh38 chr3: 10,489,410-10,585,368 , GRCh37.p13 chr3: 10,531,094-10,627,052 ATP2B2
    nsv6714081copy number variation1nstd229human GRCh38 chr3: 10,474,068-10,484,747 , GRCh37.p13 chr3: 10,515,752-10,526,431 ATP2B2
    nsv6713806copy number variation1nstd229human GRCh38 chr3: 10,568,129-10,573,037 , GRCh37.p13 chr3: 10,609,813-10,614,721 ATP2B2
    nsv6713542copy number variation1nstd229human GRCh38 chr3: 10,566,300-10,571,241 , GRCh37.p13 chr3: 10,607,984-10,612,925 ATP2B2
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