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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6715800copy number variation1nstd229human GRCh38 chr2: 241,462,667-241,628,308 , GRCh37.p13 chr2: 242,402,082-242,567,723 STK25, KCTD5P1, 8 more genes
    nsv6707014copy number variation1nstd229human GRCh38 chr2: 241,485,778-241,496,074 , GRCh37.p13 chr2: 242,425,193-242,435,489 FARP2, STK25
    nsv6636841copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,878,509-242,783,384 , GRCh38.p12 chr2: 235,969,865-241,841,232 COPS8-DT, MTND5P46, 128 more genes
    nsv6636733copy number variation1nstd102humanUncertain significance GRCh37 chr2: 242,379,032-242,783,384 , GRCh38.p12 chr2: 241,439,617-241,841,232 ATG4B, THAP4, 15 more genes
    nsv6636673copy number variation1nstd102humanPathogenic GRCh37 chr2: 235,942,616-242,783,384 , GRCh38.p12 chr2: 235,033,972-241,841,232 LINC02991, OR6B3, 136 more genes
    nsv6634398copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,229,304-243,199,373 , GRCh38.p12 chr2: 238,320,663-242,157,305 HDAC4-AS1, ING5, 92 more genes
    nsv6628029copy number variation1nstd224human GRCh37 chr2: 242,312,572-242,795,350 , GRCh38.p12 chr2: 241,373,157-241,853,198 ATG4B, ING5, 17 more genes
    nsv6348430copy number variation1nstd223human GRCh38 chr2: 237,953,314-241,782,040 , GRCh37.p13 chr2: 238,861,956-242,721,455 HDLBP-AS1, TWIST2, 90 more genes
    nsv6344528copy number variation1nstd223human GRCh38 chr2: 241,505,072-241,505,957 , GRCh37.p13 chr2: 242,444,487-242,445,372 STK25
    nsv6343320copy number variation1nstd223human GRCh38 chr2: 241,462,667-241,628,310 , GRCh37.p13 chr2: 242,402,082-242,567,725 BOK, LOC107985788, 8 more genes
    nsv6315457copy number variation1nstd102humanPathogenic GRCh37 chr2: 236,472,789-242,783,384 , GRCh38.p12 chr2: 235,564,145-241,841,232 AGAP1, OR5S1P, 130 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314846copy number variation1nstd102humanPathogenic GRCh38 chr2: 236,710,422-242,106,504 , GRCh37.p13 chr2: 237,619,065-243,048,655 LINC01937, FAM240C, 126 more genes
    nsv6311660copy number variation3nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 238,233,417-242,801,596 , GRCh38.p12 chr2: 237,324,774-241,859,444 LOC105373968, LOC100420500, 107 more genes
    nsv6311659copy number variation2nstd102humanUncertain significance GRCh37 chr2: 238,233,417-242,800,990 , GRCh38.p12 chr2: 237,324,774-241,858,838 COPS9, LOC105373977, 107 more genes
    nsv6311563copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 236,403,331-242,801,596 , GRCh38.p12 chr2: 235,494,687-241,859,444 HDAC4-AS1, COPS8-DT, 134 more genes
    nsv6291434copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,499,041-242,783,384 , GRCh38.p12 chr2: 236,590,398-241,841,232 LINC01107, COL6A3, 118 more genes
    nsv6291102copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,436,367-242,783,384 , GRCh38.p12 chr2: 238,527,726-241,841,232 MGC16025, UICLM, 74 more genes
    nsv6290725copy number variation1nstd102humanUncertain significance GRCh37 chr2: 240,208,466-243,199,373 , GRCh38.p12 chr2: 239,286,771-242,157,305 LOC107985836, RTP5, 78 more genes
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