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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096990copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,245,174-184,633,797 , GRCh38.p12 chr4: 182,324,021-183,712,644 RNU6-335P, LOC101929996, 29 more genes
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7055054inversion1nstd229human GRCh38 chr4: 177,546,174-183,679,474 , GRCh37.p13 chr4: 178,467,328-184,600,627 RNU6-479P, VTI1BP2, 52 more genes
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7050592inversion1nstd229human GRCh38 chr4: 181,219,378-183,892,493 , GRCh37.p13 chr4: 182,140,531-184,813,646 ING2, VTI1BP2, 40 more genes
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv7047440inversion1nstd229human GRCh38 chr4: 183,315,204-183,317,562 , GRCh37.p13 chr4: 184,236,357-184,238,715 CLDN22, WWC2
    nsv7042631inversion1nstd229human GRCh38 chr4: 183,104,390-183,621,127 , GRCh37.p13 chr4: 184,025,543-184,542,280 CLDN24, LOC100533630, 10 more genes
    nsv7038446inversion1nstd229human GRCh38 chr4: 182,834,579-184,176,114 , GRCh37.p13 chr4: 183,755,732-185,097,267 LOC105377581, FBLP1, 30 more genes
    nsv6738626copy number variation1nstd229human GRCh38 chr4: 183,319,419-183,346,378 , GRCh37.p13 chr4: 184,240,572-184,267,531 CLDN22, WWC2, 1 more genes
    nsv6636301copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,694,501-190,957,473 , GRCh38.p12 chr4: 182,773,348-190,036,318 LOC105377588, ENPP6, 139 more genes
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629218copy number variation1nstd224human GRCh37 chr4: 184,189,457-184,271,019 , GRCh38.p12 chr4: 183,268,304-183,349,866 CLDN24, CLDN22, 1 more genes
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
    nsv6314781copy number variation1nstd220human GRCh38.p12 chr4: 181,774,580-188,158,025 , GRCh37 chr4: 182,695,733-189,079,179 , SLC25A4, 117 more genes
    nsv6313744copy number variation1nstd102humanPathogenic GRCh37 chr4: 183,221,828-190,957,473 , GRCh38.p12 chr4: 182,300,675-190,036,318 RNU6-1053P, LINC02436, 141 more genes
    nsv6313729copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,755,174-190,225,765 , GRCh38.p12 chr4: 158,834,022-189,304,611 NAF1, LOC107986200, 336 more genes
    nsv6313663copy number variation1nstd102humanPathogenic GRCh37 chr4: 175,855,408-190,957,473 , GRCh38.p12 chr4: 174,934,257-190,036,318 LINC01596, NDUFB5P1, 190 more genes
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