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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974585insertion1nstd209human GRCh38 chr11: 103,049,766-103,049,766 , GRCh37.p13 chr11: 102,920,495-102,920,495 DCUN1D5
    nsv5970288insertion1nstd209human GRCh38 chr11: 103,072,343-103,072,343 , GRCh37.p13 chr11: 102,943,072-102,943,072 DCUN1D5
    nsv5696949mobile element insertion1nstd211human GRCh38 chr11: 103,050,354-103,050,354 , GRCh37.p13 chr11: 102,921,083-102,921,083 DCUN1D5
    nsv5672640copy number variation1nstd102humanPathogenic GRCh37 chr11: 94,153,285-111,965,700 , GRCh38.p12 chr11: 94,420,119-112,094,976 HSPD1P13, CARD17P, 239 more genes
    nsv5658333insertion1nstd207human GRCh38 chr11: 103,049,791-103,049,791 , GRCh37.p13 chr11: 102,920,520-102,920,520 DCUN1D5
    nsv5650608insertion1nstd207human GRCh38 chr11: 103,050,341-103,050,341 , GRCh37.p13 chr11: 102,921,070-102,921,070 DCUN1D5
    nsv5555653mobile element insertion1nstd206human GRCh38 chr11: 103,056,772-103,056,772 , GRCh37.p13 chr11: 102,927,501-102,927,501 DCUN1D5
    nsv5500877copy number variation1nstd206human GRCh38 chr11: 103,067,239-103,336,989 , GRCh37.p13 chr11: 102,937,968-103,207,717 DCUN1D5, DYNC2H1
    nsv5496101copy number variation1nstd206human GRCh38 chr11: 103,074,537-103,074,734 , GRCh37.p13 chr11: 102,945,266-102,945,463 DCUN1D5
    nsv5403365mobile element insertion1nstd206human GRCh38 chr11: 103,050,354-103,050,405 , GRCh37.p13 chr11: 102,921,083-102,921,134 DCUN1D5
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5131498mobile element insertion1nstd203human GRCh38 chr11: 103,050,346-103,050,354 , GRCh37.p13 chr11: 102,921,075-102,921,083 DCUN1D5
    nsv5128808mobile element insertion1nstd203human GRCh38 chr11: 103,050,341-103,050,354 , GRCh37.p13 chr11: 102,921,070-102,921,083 DCUN1D5
    nsv4980365copy number variation1nstd200human GRCh38 chr11: 103,056,015-103,057,431 , GRCh37.p13 chr11: 102,926,744-102,928,160 DCUN1D5
    nsv4714810copy number variation1nstd195human GRCh37 chr11: 102,910,401-103,007,001 , GRCh38.p12 chr11: 103,039,672-103,136,272 DYNC2H1, DCUN1D5, 1 more genes
    nsv4608540copy number variation1nstd183human GRCh37 chr11: 102,937,679-103,171,862 , GRCh38.p12 chr11: 103,066,950-103,301,133 DCUN1D5, DYNC2H1
    nsv4507911mobile element insertion1nstd166human GRCh37.p13 chr11: 102,923,849-102,923,849 , GRCh38.p12 chr11: 103,053,120-103,053,120 DCUN1D5
    nsv4502679mobile element insertion1nstd166human GRCh37.p13 chr11: 102,921,070-102,921,070 , GRCh38.p12 chr11: 103,050,341-103,050,341 DCUN1D5
    nsv4421684copy number variation1nstd174human GRCh37 chr11: 102,936,632-103,205,311 , GRCh38.p12 chr11: 103,065,903-103,334,583 DYNC2H1, DCUN1D5
    nsv4388324copy number variation1nstd173human GRCh37 chr11: 102,937,825-103,207,644 , GRCh38.p12 chr11: 103,067,096-103,336,916 DCUN1D5, DYNC2H1
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