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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046802inversion1nstd229human GRCh38 chr7: 88,777,628-89,672,258 , GRCh37.p13 chr7: 88,406,942-89,301,572 TEX47, LOC107986817, 2 more genes
    nsv6833152copy number variation1nstd229human GRCh38 chr7: 88,517,053-90,538,988 , GRCh37.p13 chr7: 88,146,368-90,168,302 LOC107986819, LOC101409256, 20 more genes
    nsv6827370copy number variation1nstd229human GRCh38 chr7: 88,494,052-90,880,306 , GRCh37.p13 chr7: 88,123,367-90,509,621 LOC105375387, CDK14, 24 more genes
    nsv6826636copy number variation1nstd229human GRCh38 chr7: 88,733,141-88,856,123 , GRCh37.p13 chr7: 88,362,455-88,485,437 ZNF804B, LOC107986816, 1 more genes
    nsv6826454copy number variation1nstd229human GRCh38 chr7: 88,729,388-88,922,359 , GRCh37.p13 chr7: 88,358,702-88,551,673 TEX47, ZNF804B, 1 more genes
    nsv6823791copy number variation1nstd229human GRCh38 chr7: 88,796,578-88,796,949 , GRCh37.p13 chr7: 88,425,892-88,426,263 ZNF804B, TEX47
    nsv6819442copy number variation1nstd229human GRCh38 chr7: 88,750,435-89,639,241 , GRCh37.p13 chr7: 88,379,749-89,268,555 LOC105375387, LOC107986817, 2 more genes
    nsv6818739copy number variation1nstd229human GRCh38 chr7: 84,598,855-91,861,148 , GRCh37.p13 chr7: 84,228,171-91,490,462 CDK14, LOC101409256, 59 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
    nsv6632464copy number variation1nstd224human GRCh37 chr7: 88,148,465-89,880,949 , GRCh38.p12 chr7: 88,519,150-90,251,635 EEF1A1P28, LOC105375387, 13 more genes
    nsv6632401copy number variation1nstd224human GRCh37 chr7: 88,423,502-89,410,098 , GRCh38.p12 chr7: 88,794,188-89,780,784 TEX47, RNU6-274P, 3 more genes
    nsv6632273copy number variation1nstd224human GRCh37 chr7: 88,161,734-89,876,365 , GRCh38.p12 chr7: 88,532,419-90,247,051 STEAP2, RNU6-274P, 13 more genes
    nsv6615887copy number variation1nstd223human GRCh38 chr7: 88,517,053-90,538,988 , GRCh37.p13 chr7: 88,146,368-90,168,302 SLC66A2P1, CFAP69, 20 more genes
    nsv6610716copy number variation1nstd223human GRCh38 chr7: 88,750,435-89,639,240 , GRCh37.p13 chr7: 88,379,749-89,268,554 LOC107986817, TEX47, 2 more genes
    nsv6603850copy number variation1nstd223human GRCh38 chr7: 88,710,380-90,258,175 , GRCh37.p13 chr7: 88,339,694-89,887,489 STEAP2, CFAP69, 10 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6137019copy number variation1nstd213human GRCh37 chr7: 88,290,000-88,650,001 , GRCh38.p12 chr7: 88,660,686-89,020,687 TEX47, ZNF804B, 1 more genes
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
    nsv6136212copy number variation1nstd213human GRCh37 chr7: 88,380,000-88,680,001 , GRCh38.p12 chr7: 88,750,686-89,050,687 TEX47, ZNF804B
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