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Items: 1 to 20 of 261

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146356insertion1nstd232human GRCh37.p13 chr4: 77,936,172-77,936,172 , GRCh38.p12 chr4: 77,015,019-77,015,019 SEPTIN11, LOC105377291
    nsv7139054insertion1nstd232human GRCh37.p13 chr4: 77,949,914-77,949,914 , GRCh38.p12 chr4: 77,028,761-77,028,761 SEPTIN11, LOC105377291
    nsv7048216inversion1nstd229human GRCh38 chr4: 76,655,869-77,303,378 , GRCh37.p13 chr4: 77,577,022-78,224,531 SUMO2P11, TXNP6, 16 more genes
    nsv7040415inversion1nstd229human GRCh38 chr4: 72,183,424-80,893,316 , GRCh37.p13 chr4: 73,049,141-81,814,470 , KPNA2P1, 148 more genes
    nsv7038331inversion1nstd229human GRCh38 chr4: 76,985,996-76,986,987 , GRCh37.p13 chr4: 77,907,149-77,908,140 SEPTIN11, LOC105377291
    nsv6757615copy number variation1nstd229human GRCh38 chr4: 76,842,072-77,130,088 , GRCh37.p13 chr4: 77,763,225-78,051,241 TXNP6, SEPTIN11, 8 more genes
    nsv6756185copy number variation1nstd229human GRCh38 chr4: 76,588,889-77,316,456 , GRCh37.p13 chr4: 77,510,042-78,237,609 LOC100421494, TXNP6, 18 more genes
    nsv6756173copy number variation1nstd229human GRCh38 chr4: 76,996,411-77,113,269 , GRCh37.p13 chr4: 77,917,564-78,034,422 RPL7P17, LOC339966, 3 more genes
    nsv6751427copy number variation1nstd229human GRCh38 chr4: 76,965,902-76,965,984 , GRCh37.p13 chr4: 77,887,055-77,887,137 SEPTIN11
    nsv6749244copy number variation1nstd229human GRCh38 chr4: 71,830,854-79,510,197 , GRCh37.p13 chr4: 72,696,571-80,431,351 , COX18, 134 more genes
    nsv6746945copy number variation1nstd229human GRCh38 chr4: 76,984,922-77,109,918 , GRCh37.p13 chr4: 77,906,075-78,031,071 CCNI, LOC105377291, 2 more genes
    nsv6745655copy number variation1nstd229human GRCh38 chr4: 76,978,066-76,983,123 , GRCh37.p13 chr4: 77,899,219-77,904,276 LOC105377291, SEPTIN11
    nsv6744697copy number variation1nstd229human GRCh38 chr4: 77,007,626-77,007,732 , GRCh37.p13 chr4: 77,928,779-77,928,885 SEPTIN11, LOC105377291
    nsv6743277copy number variation1nstd229human GRCh38 chr4: 76,967,421-76,979,522 , GRCh37.p13 chr4: 77,888,574-77,900,675 SEPTIN11, LOC105377291
    nsv6738815copy number variation1nstd229human GRCh38 chr4: 77,037,893-77,038,544 , GRCh37.p13 chr4: 77,959,046-77,959,697 SEPTIN11, LOC105377291
    nsv6630162copy number variation1nstd224human GRCh37 chr4: 77,915,665-78,053,975 , GRCh38.p12 chr4: 76,994,512-77,132,822 LOC105377291, CCNI, 3 more genes
    nsv6629735copy number variation1nstd224human GRCh37 chr4: 76,885,365-79,465,559 , GRCh38.p12 chr4: 75,964,212-78,544,405 CCNI, NUP54, 54 more genes
    nsv6571775inversion1nstd223human GRCh38 chr4: 76,985,632-76,987,235 , GRCh37.p13 chr4: 77,906,785-77,908,388 SEPTIN11, LOC105377291
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6561612inversion1nstd223human GRCh38 chr4: 76,985,996-76,986,991 , GRCh37.p13 chr4: 77,907,149-77,908,144 SEPTIN11, LOC105377291
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