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Items: 1 to 20 of 340

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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
    nsv7038446inversion1nstd229human GRCh38 chr4: 182,834,579-184,176,114 , GRCh37.p13 chr4: 183,755,732-185,097,267 LOC105377581, FBLP1, 30 more genes
    nsv6756144copy number variation1nstd229human GRCh38 chr4: 183,509,739-183,794,572 , GRCh37.p13 chr4: 184,430,892-184,715,725 ING2, LOC105377581, 8 more genes
    nsv6750088copy number variation1nstd229human GRCh38 chr4: 183,658,839-183,663,129 , GRCh37.p13 chr4: 184,579,992-184,584,282 RWDD4, TRAPPC11
    nsv6748775copy number variation1nstd229human GRCh38 chr4: 183,649,013-183,653,943 , GRCh37.p13 chr4: 184,570,166-184,575,096 RNU6-479P, RWDD4
    nsv6744773copy number variation1nstd229human GRCh38 chr4: 183,528,600-183,785,915 , GRCh37.p13 chr4: 184,449,753-184,707,068 RWDD4, LOC101929996, 6 more genes
    nsv6744656copy number variation1nstd229human GRCh38 chr4: 183,653,343-183,655,387 , GRCh37.p13 chr4: 184,574,496-184,576,540 RNU6-479P, RWDD4
    nsv6741068copy number variation1nstd229human GRCh38 chr4: 183,652,246-183,656,966 , GRCh37.p13 chr4: 184,573,399-184,578,119 RNU6-479P, RWDD4
    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
    nsv6636237copy number variation1nstd102humanUncertain significance GRCh37 chr4: 184,565,910-184,928,980 , GRCh38.p12 chr4: 183,644,757-184,007,827 TRAPPC11, RNU6-1053P, 5 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
    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
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