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Items: 1 to 20 of 41115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137782copy number variation1nstd102humanUncertain significance GRCh37 chr17: 34,171,549-34,171,632 , GRCh38 chr17: 35,844,545-35,844,628 TAF15
    nsv6137778copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr11: 108,225,602-108,239,827 , GRCh38.p12 chr11: 108,354,875-108,369,100 ATM, C11orf65
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv6137716copy number variation1nstd102humanUncertain significance GRCh37 chr11: 108,114,846-108,239,827 , GRCh38.p12 chr11: 108,244,119-108,369,100 C11orf65, ATM
    nsv6137705copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,419,493-40,774,118 , GRCh38.p12 chr9: 61,281,967-67,217,006 , GRCh38.p12 chr9: 36,419,496-39,445,729 ZNF658B, LOC105379814, 208 more genes
    nsv6137704copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,426,622-38,787,479 , GRCh38.p12 chr9: 36,426,625-38,787,482 MELK, SLC25A51, 55 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 ARHGEF39, LOC105376026, 84 more genes
    nsv6137701copy number variation1nstd102humanLikely pathogenic GRCh37 chr13: 28,669,064-31,367,407 , GRCh38.p12 chr13: 28,094,927-30,793,270 ALOX5AP, FLT1, 41 more genes
    nsv6137700copy number variation1nstd102humanPathogenic GRCh37 chr9: 36,088,563-39,092,820 , GRCh38.p12 chr9: 36,088,566-39,092,823 SNX18P3, VN1R48P, 69 more genes
    nsv6131637insertion1nstd186human GRCh37 chr16: 31,313,771-31,313,792 , GRCh38.p12 chr16: 31,302,450-31,302,471 ITGAM
    nsv6131242insertion1nstd186human GRCh37 chr17: 79,954,909-79,954,959 , GRCh38.p12 chr17: 81,997,033-81,997,083 ASPSCR1
    nsv6131072insertion1nstd186human GRCh37 chr21: 36,303,862-36,303,866 , GRCh38.p12 chr21: 34,931,565-34,931,569 RUNX1
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130602mobile element insertion1nstd186human GRCh37 chr8: 72,399,236-72,399,287 , GRCh38.p12 chr8: 71,487,001-71,487,052 EYA1
    nsv6130457insertion1nstd186human GRCh37 chr15: 80,718,429-80,718,451 , GRCh38.p12 chr15: 80,426,087-80,426,109 ARNT2
    nsv6130243insertion1nstd186human GRCh37 chr12: 102,799,045-102,799,080 , GRCh38.p12 chr12: 102,405,267-102,405,302 IGF1, LINC02456
    nsv6130012insertion1nstd186human GRCh37 chr17: 79,967,505-79,967,512 , GRCh38.p12 chr17: 82,009,629-82,009,636 ASPSCR1
    nsv6129369insertion1nstd186human GRCh37 chr19: 2,183,925-2,183,925 , GRCh38.p12 chr19: 2,183,926-2,183,926 DOT1L
    nsv6127496insertion1nstd186human GRCh37 chrY: 13,193,955-58,979,440 , GRCh38.p12 chrY: 11,038,279-56,833,293 , ELOCP10, 371 more genes
    nsv6125973copy number variation1nstd186human GRCh37 chr21: 36,298,782-36,298,854 , GRCh38.p12 chr21: 34,926,485-34,926,557 RUNX1
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