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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv6835379copy number variation1nstd229human GRCh38 chr7: 77,684,818-77,692,597 , GRCh37.p13 chr7: 77,314,135-77,321,914 APTR
    nsv6834660copy number variation1nstd229human GRCh38 chr7: 77,670,870-77,673,091 , GRCh37.p13 chr7: 77,300,187-77,302,408 LOC105375363, APTR
    nsv6834448copy number variation1nstd229human GRCh38 chr7: 77,693,001-77,695,200 , GRCh37.p13 chr7: 77,322,318-77,324,517 APTR, RSBN1L
    nsv6828604copy number variation1nstd229human GRCh38 chr7: 77,567,405-77,745,003 , GRCh37.p13 chr7: 77,196,722-77,374,320 LOC105375363, RSBN1L, 2 more genes
    nsv6825143copy number variation1nstd229human GRCh38 chr7: 77,613,695-77,716,233 , GRCh37.p13 chr7: 77,243,012-77,345,550 PTPN12, RSBN1L, 2 more genes
    nsv6821531copy number variation1nstd229human GRCh38 chr7: 77,670,325-77,677,395 , GRCh37.p13 chr7: 77,299,642-77,306,712 LOC105375363, APTR
    nsv6821375copy number variation1nstd229human GRCh38 chr7: 77,674,870-77,757,851 , GRCh37.p13 chr7: 77,304,187-77,387,168 LOC105375363, RSBN1L, 1 more genes
    nsv6820288copy number variation1nstd229human GRCh38 chr7: 77,676,863-77,687,060 , GRCh37.p13 chr7: 77,306,180-77,316,377 LOC105375363, APTR
    nsv6818758copy number variation1nstd229human GRCh38 chr7: 77,676,199-77,676,230 , GRCh37.p13 chr7: 77,305,516-77,305,547 LOC105375363, APTR
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 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
    nsv6618608copy number variation1nstd223human GRCh38 chr7: 77,693,001-77,694,829 , GRCh37.p13 chr7: 77,322,318-77,324,146 APTR, RSBN1L
    nsv6615787copy number variation1nstd223human GRCh38 chr7: 77,684,801-77,692,600 , GRCh37.p13 chr7: 77,314,118-77,321,917 APTR
    nsv6611614copy number variation1nstd223human GRCh38 chr7: 77,676,641-77,677,081 , GRCh37.p13 chr7: 77,305,958-77,306,398 APTR, LOC105375363
    nsv6605556copy number variation1nstd223human GRCh38 chr7: 77,670,870-77,673,088 , GRCh37.p13 chr7: 77,300,187-77,302,405 APTR, LOC105375363
    nsv6605237copy number variation1nstd223human GRCh38 chr7: 77,641,392-77,676,965 , GRCh37.p13 chr7: 77,270,709-77,306,282 LOC105375363, APTR
    nsv6600459copy number variation1nstd223human GRCh38 chr7: 77,696,772-77,700,070 , GRCh37.p13 chr7: 77,326,089-77,329,387 RSBN1L, APTR
    nsv6566878inversion1nstd223human GRCh38 chr7: 77,679,176-77,679,541 , GRCh37.p13 chr7: 77,308,493-77,308,858 LOC105375363, APTR
    nsv6564016inversion1nstd223human GRCh38 chr7: 77,659,924-77,660,698 , GRCh37.p13 chr7: 77,289,241-77,290,015 APTR, LOC105375363
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