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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097614copy number variation1nstd102humanUncertain significance GRCh37 chr7: 16,131,320-17,382,688 , GRCh38.p12 chr7: 16,091,695-17,343,064 BRWD1P3, ANKMY2, 19 more genes
    nsv7048011inversion1nstd229human GRCh38 chr7: 16,867,829-16,903,477 , GRCh37.p13 chr7: 16,907,453-16,943,101 AGR3, LOC100131425
    nsv7047529inversion1nstd229human GRCh38 chr7: 16,868,044-16,910,685 , GRCh37.p13 chr7: 16,907,668-16,950,309 LOC100131425, AGR3
    nsv7038576inversion1nstd229human GRCh38 chr7: 16,300,700-17,558,371 , GRCh37.p13 chr7: 16,340,325-17,597,995 LOC317727, LOC105375170, 21 more genes
    nsv6814097copy number variation1nstd229human GRCh38 chr7: 16,798,427-17,711,088 , GRCh37.p13 chr7: 16,838,051-17,750,712 LOC100131425, LINC02888, 12 more genes
    nsv6814066copy number variation1nstd229human GRCh38 chr7: 16,875,809-17,377,161 , GRCh37.p13 chr7: 16,915,433-17,416,785 AHR, LOC107986772, 7 more genes
    nsv6812072copy number variation1nstd229human GRCh38 chr7: 16,805,172-16,943,197 , GRCh37.p13 chr7: 16,844,796-16,982,821 LOC100131425, AGR2, 3 more genes
    nsv6810871copy number variation1nstd229human GRCh38 chr7: 16,504,503-17,165,581 , GRCh37.p13 chr7: 16,544,128-17,205,205 LRRC72, LOC105375169, 13 more genes
    nsv6809341copy number variation1nstd229human GRCh38 chr7: 16,889,190-16,892,058 , GRCh37.p13 chr7: 16,928,814-16,931,682 LOC100131425
    nsv6808986copy number variation1nstd229human GRCh38 chr7: 16,804,547-16,886,652 , GRCh37.p13 chr7: 16,844,171-16,926,276 AGR3, AGR2, 3 more genes
    nsv6807204copy number variation1nstd229human GRCh38 chr7: 16,822,353-16,907,707 , GRCh37.p13 chr7: 16,861,977-16,947,331 LOC100131425, RAD17P1, 2 more genes
    nsv6805099copy number variation1nstd229human GRCh38 chr7: 16,810,933-16,968,652 , GRCh37.p13 chr7: 16,850,557-17,008,276 AGR3, LOC100131425, 2 more genes
    nsv6804910copy number variation1nstd229human GRCh38 chr7: 16,787,647-16,977,542 , GRCh37.p13 chr7: 16,827,271-17,017,166 AGR2, LOC100287613, 3 more genes
    nsv6803974copy number variation1nstd229human GRCh38 chr7: 16,839,944-17,849,438 , GRCh37.p13 chr7: 16,879,568-17,889,061 AGR3, LOC105375172, 12 more genes
    nsv6803309copy number variation1nstd229human GRCh38 chr7: 16,833,201-16,904,800 , GRCh37.p13 chr7: 16,872,825-16,944,424 LOC100131425, AGR3, 2 more genes
    nsv6799404copy number variation1nstd229human GRCh38 chr7: 16,359,233-17,380,982 , GRCh37.p13 chr7: 16,398,858-17,420,606 LOC101927609, SOSTDC1, 19 more genes
    nsv6798408copy number variation1nstd229human GRCh38 chr7: 16,886,901-16,889,200 , GRCh37.p13 chr7: 16,926,525-16,928,824 LOC100131425
    nsv6637135copy number variation1nstd102humanUncertain significance GRCh37 chr7: 15,639,869-16,963,424 , GRCh38.p12 chr7: 15,600,244-16,923,800 LOC105375166, LOC105375169, 20 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 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
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