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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3167255copy number variation2nstd151human GRCh37 (hg19) chr20: 2,641,100-2,644,839 , GRCh38 (hg38) chr20: 2,660,454-2,664,193 IDH3B
    nsv3166516copy number variation1nstd151human GRCh37 (hg19) chr20: 2,641,340-2,644,839 , GRCh38 (hg38) chr20: 2,660,694-2,664,193 IDH3B
    nsv3166394copy number variation2nstd151human GRCh37 (hg19) chr20: 2,640,673-2,644,839 , GRCh38 (hg38) chr20: 2,660,027-2,664,193 IDH3B
    nsv3165981copy number variation1nstd151human GRCh37 (hg19) chr22: 41,903,792-41,940,110 , GRCh38 (hg38) chr22: 41,507,788-41,544,106 POLR3H, ACO2
    nsv3165812copy number variation1nstd151human GRCh37 (hg19) chr20: 2,640,673-2,644,217 , GRCh38 (hg38) chr20: 2,660,027-2,663,571 IDH3B
    nsv3165582copy number variation1nstd151human GRCh37 (hg19) chr20: 2,644,089-2,644,656 , GRCh38 (hg38) chr20: 2,663,443-2,664,010 IDH3B
    nsv3165561copy number variation1nstd151human GRCh37 (hg19) chr20: 2,641,550-2,644,656 , GRCh38 (hg38) chr20: 2,660,904-2,664,010 IDH3B
    nsv3165306copy number variation3nstd151human GRCh37 (hg19) chr20: 2,644,568-2,644,839 , GRCh38 (hg38) chr20: 2,663,922-2,664,193 IDH3B
    nsv3164955copy number variation2nstd151human GRCh37 (hg19) chr20: 2,640,342-2,644,839 , GRCh38 (hg38) chr20: 2,659,696-2,664,193 IDH3B
    nsv3164902copy number variation1nstd151human GRCh37 (hg19) chr20: 2,640,673-2,641,620 , GRCh38 (hg38) chr20: 2,660,027-2,660,974 IDH3B
    nsv3164673copy number variation1nstd151human GRCh37 (hg19) chr17: 40,024,060-40,120,763 , GRCh38 (hg38) chr17: 41,867,807-41,968,745 CNP, ACLY, 1 more genes
    nsv3163507copy number variation1nstd151human GRCh37 (hg19) chr20: 56,063,445-56,191,529 , GRCh38 (hg38) chr20: 57,488,389-57,616,473 CTCFL, PCK1, 1 more genes
    nsv3163325copy number variation1nstd151human GRCh37 (hg19) chr22: 41,911,378-41,928,754 , GRCh38 (hg38) chr22: 41,515,374-41,532,750 POLR3H, ACO2
    nsv3163172copy number variation7nstd151human GRCh37 (hg19) chr20: 2,644,089-2,644,839 , GRCh38 (hg38) chr20: 2,663,443-2,664,193 IDH3B
    nsv3162817copy number variation1nstd151human GRCh37 (hg19) chr22: 41,918,831-41,940,110 , GRCh38 (hg38) chr22: 41,522,827-41,544,106 POLR3H, ACO2
    nsv3162732copy number variation1nstd151human GRCh37 (hg19) chr17: 40,034,353-40,180,267 , GRCh38 (hg38) chr17: 41,878,100-42,028,249 CNP, ZNF385C, 4 more genes
    nsv3162671copy number variation3nstd151human GRCh37 (hg19) chr22: 41,924,480-41,928,754 , GRCh38 (hg38) chr22: 41,528,476-41,532,750 POLR3H, ACO2
    nsv3162396copy number variation1nstd151human GRCh37 (hg19) chr20: 2,639,085-2,644,839 , GRCh38 (hg38) chr20: 2,658,439-2,664,193 IDH3B
    nsv3162193copy number variation1nstd151human GRCh37 (hg19) chr20: 2,361,612-2,644,656 , GRCh38 (hg38) chr20: 2,380,966-2,664,010 SNORD119, MIR1292, 11 more genes
    nsv3161824copy number variation1nstd151human GRCh37 (hg19) chr20: 2,644,303-2,644,839 , GRCh38 (hg38) chr20: 2,663,657-2,664,193 IDH3B
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