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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116070mobile element insertion1nstd186human GRCh37 chr15: 79,167,153-79,167,153 , GRCh38.p12 chr15: 78,874,811-78,874,811 MORF4L1
    nsv5978620insertion1nstd209human GRCh38 chr15: 78,874,811-78,874,811 , GRCh37.p13 chr15: 79,167,153-79,167,153 MORF4L1
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5932118copy number variation1nstd209human GRCh38 chr15: 78,876,651-78,876,733 , GRCh37.p13 chr15: 79,168,993-79,169,075 MORF4L1
    nsv5694605mobile element insertion2nstd211human GRCh38 chr15: 78,874,827-78,874,827 , GRCh37.p13 chr15: 79,167,169-79,167,169 MORF4L1
    nsv5660434insertion1nstd207human GRCh38 chr15: 78,874,811-78,874,811 , GRCh37.p13 chr15: 79,167,153-79,167,153 MORF4L1
    nsv5531656copy number variation1nstd206human GRCh38 chr15: 78,876,653-78,876,734 , GRCh37.p13 chr15: 79,168,995-79,169,076 MORF4L1
    nsv5416139mobile element insertion1nstd206human GRCh38 chr15: 78,874,811-78,874,811 , GRCh37.p13 chr15: 79,167,153-79,167,153 MORF4L1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5349205translocation1nstd200human GRCh38 chr15: 78,876,734-78,876,734 , GRCh38 chr15: 78,876,653-78,876,653 , GRCh37.p13 chr15: 79,168,995-79,168,995 , GRCh37.p13 chr15: 79,169,076-79,169,076 MORF4L1
    nsv5159507mobile element insertion1nstd203human GRCh38 chr15: 78,874,775-78,874,811 , GRCh37.p13 chr15: 79,167,117-79,167,153 MORF4L1
    nsv5152278mobile element insertion1nstd203human GRCh38 chr15: 78,875,609-78,875,644 , GRCh37.p13 chr15: 79,167,951-79,167,986 MORF4L1
    nsv5151819mobile element insertion1nstd203human GRCh38 chr15: 78,874,811-78,874,827 , GRCh37.p13 chr15: 79,167,153-79,167,169 MORF4L1
    nsv5148197mobile element insertion1nstd203human GRCh38 chr15: 78,874,816-78,874,827 , GRCh37.p13 chr15: 79,167,158-79,167,169 MORF4L1
    nsv5145774mobile element insertion1nstd203human GRCh38 chr15: 78,874,777-78,874,811 , GRCh37.p13 chr15: 79,167,119-79,167,153 MORF4L1
    nsv5143496mobile element insertion1nstd203human GRCh38 chr15: 78,874,810-78,874,827 , GRCh37.p13 chr15: 79,167,152-79,167,169 MORF4L1
    nsv5142884mobile element insertion1nstd203human GRCh38 chr15: 78,874,818-78,874,827 , GRCh37.p13 chr15: 79,167,160-79,167,169 MORF4L1
    nsv5141548mobile element insertion1nstd203human GRCh38 chr15: 78,874,598-78,874,601 , GRCh37.p13 chr15: 79,166,940-79,166,943 MORF4L1
    nsv5001890copy number variation1nstd200human GRCh38 chr15: 78,868,134-78,871,256 , GRCh37.p13 chr15: 79,160,476-79,163,598 MORF4L1
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