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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148111copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,742,396-28,567,325 , GRCh38.p12 chr15: 23,319,714-28,322,179 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD116-18, PWAR4, 246 more genes
    nsv7148097copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,605,427-28,566,579 , GRCh38.p12 chr15: 23,360,280-28,321,433 LOC107984770, SNORD115-31, 147 more genes
    nsv7137213copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,421-30,386,398 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-30,094,195 TVP23BP1, SNORD115-1, 247 more genes
    nsv7137100copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,691-28,566,579 , GRCh38.p12 chr15: 23,439,544-28,321,433 DMAC1P1, SNORD116-16, 142 more genes
    nsv7098883copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,406,271-28,566,579 , GRCh38.p12 chr15: 23,319,714-28,321,433 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC105370739, SNORD116-27, 246 more genes
    nsv7094276copy number variation1nstd102humanPathogenic GRCh37 chr15: 26,107,444-28,230,334 , GRCh38.p12 chr15: 25,862,297-27,985,188 GABRA5, RPL9P26, 20 more genes
    nsv7093407copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,525-28,544,662 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,299,516 UBE2CP4, SERPINE4P, 246 more genes
    nsv7093400copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,684,645-28,566,612 , GRCh38.p12 chr15: 23,439,498-28,321,466 SNORD115-45, SNORD107, 142 more genes
    nsv7067542inversion1nstd229human GRCh38 chr15: 23,549,781-28,456,830 , GRCh37.p13 chr15: 23,794,928-28,701,976 SNORD115-34, LOC107984787, 148 more genes
    nsv7065496inversion1nstd229human GRCh38 chr15: 20,672,644-28,900,286 , GRCh37.p13 chr15: 20,877,973-29,145,432 SNURF, LOC101060118, 290 more genes
    nsv7065294inversion1nstd229human GRCh38 chr15: 27,010,857-29,330,650 , GRCh37.p13 chr15: 27,256,004-29,622,854 GABRG3-AS1, HERC2P1, 40 more genes
    nsv6975202copy number variation1nstd229human GRCh38 chr15: 27,158,601-27,164,600 , GRCh37.p13 chr15: 27,403,748-27,409,747 GABRG3, GABRG3-AS1
    nsv6973165copy number variation1nstd229human GRCh38 chr15: 23,199,056-28,429,484 , GRCh37.p13 chr15: 23,564,855-28,674,630 LOC102723564, SNORD115-2, 162 more genes
    nsv6971855copy number variation1nstd229human GRCh38 chr15: 27,158,001-27,165,900 , GRCh37.p13 chr15: 27,403,148-27,411,047 GABRG3, GABRG3-AS1
    nsv6969909copy number variation1nstd229human GRCh38 chr15: 27,158,058-27,164,640 , GRCh37.p13 chr15: 27,403,205-27,409,787 GABRG3-AS1, GABRG3
    nsv6969131copy number variation1nstd229human GRCh38 chr15: 22,744,959-28,819,371 , GRCh37.p13 chr15: 23,564,855-29,064,517 RNA5SP391, PDCD6IPP1, 195 more genes
    nsv6959676copy number variation1nstd229human GRCh38 chr15: 27,158,101-27,164,600 , GRCh37.p13 chr15: 27,403,248-27,409,747 GABRG3-AS1, GABRG3
    nsv6637850copy number variation1nstd102humanUncertain significance GRCh37 chr15: 27,265,912-27,757,627 , GRCh38.p12 chr15: 27,020,765-27,512,481 RNA5SP391, LOC100420466, 4 more genes
    nsv6637778copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,770,422-28,545,601 , GRCh38.p12 chr15: 23,319,714-28,300,455 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC107984779, ULK4P1, 246 more genes
    nsv6637596copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,290,787-28,560,269 , GRCh38.p12 chr15: 23,319,714-28,315,123 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 SNORD115-23, DEPDC1P1, 246 more genes
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