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Items: 1 to 20 of 286

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049218inversion1nstd229human GRCh38 chr7: 74,874,740-75,023,295 , GRCh37.p13 chr7|NW_003871064.1: 2,403,976-2,552,531 , GRCh37.p13 chr7: 74,290,834-74,437,406 PMS2P5, CASTOR2, 3 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
    nsv6616937copy number variation1nstd223human GRCh38 chr7: 74,920,901-74,926,800 , GRCh37.p13 chr7: 74,335,929-74,341,807 , GRCh37.p13 chr7|NW_003871064.1: 2,450,137-2,456,036 PMS2P5
    nsv6610970copy number variation1nstd223human GRCh38 chr7: 74,920,001-74,925,300 , GRCh37.p13 chr7: 74,335,030-74,340,307 , GRCh37.p13 chr7|NW_003871064.1: 2,449,237-2,454,536 PMS2P5
    nsv6607008copy number variation1nstd223human GRCh38 chr7: 74,920,601-74,922,300 , GRCh37.p13 chr7: 74,335,629-74,337,328 , GRCh37.p13 chr7|NW_003871064.1: 2,449,837-2,451,536 PMS2P5
    nsv6604243copy number variation1nstd223human GRCh38 chr7: 74,890,001-74,891,200 , GRCh37.p13 chr7: 74,306,122-74,307,319 , GRCh37.p13 chr7|NW_003871064.1: 2,419,237-2,420,436 STAG3L2, PMS2P5
    nsv6601201copy number variation1nstd223human GRCh38 chr7: 74,906,801-74,908,100 , GRCh37.p13 chr7: 74,322,906-74,324,205 , GRCh37.p13 chr7|NW_003871064.1: 2,436,037-2,437,336 PMS2P5, SPDYE12
    nsv6315397copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,589,515-74,629,034 , GRCh38.p12 chr7: 73,175,475-75,175,451 MIR10525, GTF2I, 52 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6304386copy number variation1nstd186human GRCh37 chr7: 74,326,879-74,333,533 , GRCh38.p12 chr7: 74,910,779-74,918,500 PMS2P5, SPDYE12
    nsv6302642copy number variation1nstd186human GRCh37 chr7: 74,326,879-74,357,366 , GRCh38.p12 chr7: 74,910,779-74,942,389 SPDYE12, PMS2P5
    nsv6302560copy number variation1nstd186human GRCh37 chr7: 74,284,809-74,312,506 , GRCh38.p12 chr7: 74,868,719-74,896,389 PMS2P5, STAG3L2
    nsv6301789copy number variation1nstd186human GRCh37 chr7: 74,320,884-74,342,006 , GRCh38.p12 chr7: 74,904,779-74,927,000 SPDYE12, PMS2P5
    nsv6141939copy number variation1nstd206human GRCh38 chr7: 74,896,779-74,902,779 , GRCh37.p13 chr7|NW_003871064.1: 2,426,015-2,432,015 , GRCh37.p13 chr7: 74,312,896-74,318,893 PMS2P5, SPDYE12
    nsv6141744copy number variation1nstd206human GRCh38 chr7: 74,910,779-74,918,500 , GRCh37.p13 chr7: 74,326,879-74,333,533 , GRCh37.p13 chr7|NW_003871064.1: 2,440,015-2,447,736 PMS2P5, SPDYE12
    nsv6141718copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 2,384,015-2,490,015 , GRCh38 chr7: 74,854,779-74,960,779 , GRCh37.p13 chr7: 74,284,809-74,375,488 PMS2P5, STAG3L2, 2 more genes
    nsv6141643copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 2,414,015-2,432,015 , GRCh38 chr7: 74,884,779-74,902,779 , GRCh37.p13 chr7: 74,300,893-74,318,893 STAG3L2, PMS2P5, 1 more genes
    nsv6141605copy number variation1nstd206human GRCh38 chr7: 74,885,389-74,897,944 , GRCh37.p13 chr7: 74,301,503-74,314,060 , GRCh37.p13 chr7|NW_003871064.1: 2,414,625-2,427,180 STAG3L2, PMS2P5
    nsv6141413copy number variation1nstd206human GRCh38 chr7: 74,884,779-74,896,950 , GRCh37.p13 chr7|NW_003871064.1: 2,414,015-2,426,186 , GRCh37.p13 chr7: 74,300,893-74,313,066 PMS2P5, STAG3L2
    nsv6136201copy number variation1nstd213human GRCh37 chr7: 72,600,000-74,410,001 , GRCh38.p12 chr7: 73,185,960-74,984,489 GTF2I, EIF4H, 49 more genes
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