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Items: 1 to 20 of 356

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112669copy number variation1nstd102humanUncertain significance GRCh38 chr15: 28,694,170-30,078,717 , GRCh37.p13 chr15: 28,939,316-30,370,920 TUBBP8, LOC100420707, 19 more genes
    nsv5672660copy number variation1nstd102humanPathogenic GRCh38 chr15: 22,804,175-30,375,696 , GRCh37.p13 chr15: 23,564,855-30,667,899 TUBBP8, LOC102723564, 218 more genes
    nsv5277830copy number variation1nstd204human GRCh38.p13 chr15: 29,269,495-29,307,475 , GRCh37.p13 chr15: 29,561,699-29,599,679 ENTREP2, NSMCE3
    nsv5200367copy number variation1nstd102humanPathogenic GRCh37 chr15: 23,208,842-28,525,460 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,280,314 SNORD115-27, LOC105370747, 246 more genes
    nsv5005232copy number variation1nstd200human GRCh38 chr15: 29,263,149-29,285,280 , GRCh37.p13 chr15: 29,555,353-29,577,484 ENTREP2, NSMCE3
    nsv5001066copy number variation1nstd200human GRCh38 chr15: 29,260,513-29,263,527 , GRCh37.p13 chr15: 29,552,717-29,555,731 NSMCE3, ENTREP2
    nsv5001041copy number variation1nstd200human GRCh38 chr15: 28,746,353-29,391,878 , GRCh37.p13 chr15: 28,991,499-29,684,082 LOC100129687, APBA2, 9 more genes
    nsv4855691copy number variation1nstd200human GRCh37 chr15: 28,991,499-29,684,082 , GRCh38.p12 chr15|NW_011332701.1: 908,356-1,554,896 , GRCh38.p12 chr15: 28,746,353-29,391,878 , GRCh38.p12 chr15|NT_187660.1: 1,022,142-1,667,380 ENTREP2, LOC100129687, 9 more genes
    nsv4768364copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,940,039-30,366,124 , GRCh38.p12 chr15|NW_011332701.1: 856,895-2,246,641 , GRCh38.p12 chr15|NT_187660.1: 970,681-2,359,125 , GRCh38.p12 chr15: 28,694,893-30,073,921 RN7SL719P, ENTREP2, 19 more genes
    nsv4749247copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,700,525 , GRCh38.p12 chr15: 28,914,297-34,408,324 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , HNRNPA1P71, 132 more genes
    nsv4742703copy number variation1nstd199human GRCh37 chr15: 29,159,443-34,846,747 , GRCh38.p12 chr15: 28,914,297-34,554,546 , GRCh38.p12 chr15|NT_187660.1: 1,192,197-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 1,079,713-4,998,962 , KATNBL1, 138 more genes
    nsv4729372copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,915,863-32,446,830 , GRCh38.p12 chr15: 28,670,717-32,154,629 GOLGA8H, RN7SL469P, 72 more genes
    nsv4729174copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,976,540-30,386,553 , GRCh38.p12 chr15: 28,731,394-30,094,350 , GRCh38.p12 chr15|NW_011332701.1: 893,399-2,267,070 , GRCh38.p12 chr15|NT_187660.1: 1,007,185-2,379,554 NSMCE3, LOC100129687, 19 more genes
    nsv4729149copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,709,714-34,506,805 , GRCh38.p12 chr15: 28,464,568-34,214,604 APBA2, CHRM5, 125 more genes
    nsv4685744copy number variation1nstd102humannot provided GRCh37 chr15: 28,958,779-30,386,553 , GRCh38.p12 chr15|NW_011332701.1: 875,635-2,267,070 , GRCh38.p12 chr15: 28,713,633-30,094,350 , GRCh38.p12 chr15|NT_187660.1: 989,421-2,379,554 GOLGA8J, LOC105370743, 19 more genes
    nsv4685685copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,646,692-28,964,445 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , GRCh38.p12 chr15: 23,319,714-28,719,299 MKRN3, RN7SL469P, 247 more genes
    nsv4685661copy number variation1nstd102humanPathogenic GRCh37 chr15: 22,833,416-28,566,671 , GRCh38.p12 chr15: 23,319,714-28,321,525 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 LOC101060587, MPHOSPH10P8, 246 more genes
    nsv4684444copy number variation1nstd192human GRCh38.p12 chr15: 23,319,714-28,097,771 , GRCh37 chr15: 22,927,167-28,342,917 , GRCh38.p12 chr15|NW_011332701.1: 1-4,542,614 , APBA2, 258 more genes
    nsv4684244copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,962,131-32,620,127 , GRCh38.p12 chr15: 28,716,985-32,327,926 LOC644110, DNM1P28, 71 more genes
    nsv4679328copy number variation1nstd189human GRCh37.p13 chr15: 28,751,724-30,478,655 , GRCh38.p12 chr15: 28,506,578-30,186,452 , GRCh38.p12 chr15|NT_187660.1: 782,375-2,471,400 , GRCh38.p12 chr15|NW_011332701.1: 668,589-2,358,916 APBA2, TJP1, 37 more genes
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