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Items: 1 to 20 of 345

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142382insertion1nstd232human GRCh37.p13 chr7: 77,354,731-77,354,731 , GRCh38.p12 chr7: 77,725,414-77,725,414 RSBN1L
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv6834448copy number variation1nstd229human GRCh38 chr7: 77,693,001-77,695,200 , GRCh37.p13 chr7: 77,322,318-77,324,517 APTR, RSBN1L
    nsv6832416copy number variation1nstd229human GRCh38 chr7: 77,699,501-77,734,900 , GRCh37.p13 chr7: 77,328,818-77,364,217 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
    nsv6826829copy number variation1nstd229human GRCh38 chr7: 77,781,009-77,781,182 , GRCh37.p13 chr7: 77,410,326-77,410,499 RSBN1L
    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
    nsv6824356copy number variation1nstd229human GRCh38 chr7: 77,712,081-77,730,157 , GRCh37.p13 chr7: 77,341,398-77,359,474 RSBN1L
    nsv6823866copy number variation1nstd229human GRCh38 chr7: 77,758,454-77,764,564 , GRCh37.p13 chr7: 77,387,771-77,393,881 RSBN1L
    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
    nsv6819241copy number variation1nstd229human GRCh38 chr7: 77,707,968-77,724,716 , GRCh37.p13 chr7: 77,337,285-77,354,033 RSBN1L
    nsv6819122copy number variation1nstd229human GRCh38 chr7: 77,724,779-77,724,921 , GRCh37.p13 chr7: 77,354,096-77,354,238 RSBN1L
    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
    nsv6632392copy number variation1nstd224human GRCh37 chr7: 77,408,295-77,463,843 , GRCh38.p12 chr7: 77,778,978-77,834,526 PHTF2, RSBN1L, 1 more genes
    nsv6618608copy number variation1nstd223human GRCh38 chr7: 77,693,001-77,694,829 , GRCh37.p13 chr7: 77,322,318-77,324,146 APTR, RSBN1L
    nsv6616395copy number variation1nstd223human GRCh38 chr7: 77,725,382-77,725,724 , GRCh37.p13 chr7: 77,354,699-77,355,041 RSBN1L
    nsv6609832copy number variation1nstd223human GRCh38 chr7: 77,776,701-77,778,200 , GRCh37.p13 chr7: 77,406,018-77,407,517 RSBN1L
    nsv6602930copy number variation1nstd223human GRCh38 chr7: 77,758,454-77,764,559 , GRCh37.p13 chr7: 77,387,771-77,393,876 RSBN1L
    nsv6600459copy number variation1nstd223human GRCh38 chr7: 77,696,772-77,700,070 , GRCh37.p13 chr7: 77,326,089-77,329,387 RSBN1L, APTR
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