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Items: 1 to 20 of 71076

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137761copy number variation1nstd102humanLikely benign GRCh37 chrX: 53,672,687-53,672,691 , GRCh38.p12 chrX: 53,645,735-53,645,748 HUWE1
    nsv6137733copy number variation1nstd102humanBenign GRCh37 chrX: 53,672,673-53,672,676 , GRCh38.p12 chrX: 53,645,721-53,645,724 HUWE1
    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
    nsv6137723copy number variation1nstd102humanBenign GRCh37 chr16: 729,959-730,023 , GRCh38 chr16: 679,959-680,023 JMJD8, STUB1, 1 more genes
    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
    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
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6131274insertion1nstd186human GRCh37 chr16: 81,424,573-81,424,588 , GRCh38.p12 chr16: 81,390,968-81,390,983 GAN
    nsv6131051insertion1nstd186human GRCh37 chr12: 117,589,820-117,589,820 , GRCh38.p12 chr12: 117,152,015-117,152,015 FBXO21
    nsv6130935insertion1nstd186human GRCh37 chr17: 45,651,435-45,651,468 , GRCh38.p12 chr17: 47,574,069-47,574,102 NPEPPS
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130807mobile element insertion1nstd186human GRCh37 chr6: 162,181,268-162,181,319 , GRCh38.p12 chr6: 161,760,236-161,760,287 PRKN
    nsv6130307insertion1nstd186human GRCh37 chr15: 56,247,217-56,247,224 , GRCh38.p12 chr15: 55,955,019-55,955,026 NEDD4
    nsv6130064insertion1nstd186human GRCh37 chr14: 105,714,918-105,714,932 , GRCh38.p12 chr14: 105,248,581-105,248,595 BRF1, BTBD6
    nsv6130039insertion1nstd186human GRCh37 chr17: 78,289,569-78,289,569 , GRCh38.p12 chr17: 80,315,769-80,315,769 RNF213
    nsv6129974insertion1nstd186human GRCh37 chr13: 76,214,314-76,214,350 , GRCh38.p12 chr13: 75,640,178-75,640,214 LMO7
    nsv6129427insertion1nstd186human GRCh37 chr18: 71,785,675-71,785,703 , GRCh38.p12 chr18: 74,118,440-74,118,468 FBXO15
    nsv6129238insertion1nstd186human GRCh37 chr15: 25,621,915-25,621,928 , GRCh38.p12 chr15: 25,376,768-25,376,781 UBE3A, SNHG14
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