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Items: 1 to 20 of 258

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093374copy number variation1nstd102humannot provided GRCh37 chr7: 7,516,346-8,018,481 , GRCh38.p12 chr7: 7,476,715-7,978,850 CCNB2P1, GLCCI1-DT, 11 more genes
    nsv7051823inversion1nstd229human GRCh38 chr7: 6,997,578-9,925,631 , GRCh37.p13 chr7: 7,037,209-9,965,263 C1GALT1, LOC107986764, 29 more genes
    nsv7050632inversion1nstd229human GRCh38 chr7: 5,826,142-8,041,237 , GRCh37.p13 chr7: 5,865,773-8,080,867 LOC105375138, DAGLB, 57 more genes
    nsv6816339copy number variation1nstd229human GRCh38 chr7: 7,387,696-7,838,710 , GRCh37.p13 chr7: 7,427,327-7,878,341 MIOS-DT, COL28A1, 6 more genes
    nsv6815959copy number variation1nstd229human GRCh38 chr7: 7,484,645-7,877,556 , GRCh37.p13 chr7: 7,524,276-7,917,187 MIOS-DT, LOC100533631, 6 more genes
    nsv6815376copy number variation1nstd229human GRCh38 chr7: 7,391,651-7,613,685 , GRCh37.p13 chr7: 7,431,282-7,653,316 COL28A1, MIOS, 1 more genes
    nsv6811641copy number variation1nstd229human GRCh38 chr7: 7,529,997-7,615,209 , GRCh37.p13 chr7: 7,569,628-7,654,840 MIOS, COL28A1, 1 more genes
    nsv6808637copy number variation1nstd229human GRCh38 chr7: 7,577,389-7,589,513 , GRCh37.p13 chr7: 7,617,020-7,629,144 MIOS
    nsv6807147copy number variation1nstd229human GRCh38 chr7: 7,576,415-7,581,139 , GRCh37.p13 chr7: 7,616,046-7,620,770 MIOS
    nsv6807118copy number variation1nstd229human GRCh38 chr7: 7,563,084-7,565,787 , GRCh37.p13 chr7: 7,602,715-7,605,418 MIOS, MIOS-DT
    nsv6806437copy number variation1nstd229human GRCh38 chr7: 7,555,001-7,571,000 , GRCh37.p13 chr7: 7,594,632-7,610,631 MIOS, MIOS-DT
    nsv6800548copy number variation1nstd229human GRCh38 chr7: 7,576,915-7,579,996 , GRCh37.p13 chr7: 7,616,546-7,619,627 MIOS
    nsv6799541copy number variation1nstd229human GRCh38 chr7: 7,548,330-7,641,553 , GRCh37.p13 chr7: 7,587,961-7,681,184 RPA3, MIOS-DT, 2 more genes
    nsv6636555copy number variation1nstd102humanUncertain significance GRCh37 chr7: 7,617,834-7,677,809 , GRCh38.p12 chr7: 7,578,203-7,638,178 RPA3, MIOS
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634339copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-9,649,794 , GRCh38.p12 chr7: 43,360-9,610,164 MRM2, FOXL3, 182 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632377copy number variation1nstd224human GRCh37 chr7: 7,514,235-7,613,118 , GRCh38.p12 chr7: 7,474,604-7,573,487 MIOS-DT, MIOS, 1 more genes
    nsv6631940copy number variation1nstd224human GRCh37 chr7: 7,528,385-7,913,945 , GRCh38.p12 chr7: 7,488,754-7,874,314 RPA3, MIOS, 6 more genes
    nsv6617583copy number variation1nstd223human GRCh38 chr7: 7,608,301-7,609,300 , GRCh37.p13 chr7: 7,647,932-7,648,931 MIOS
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