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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 ZG16, TBX6, 45 more genes
    nsv6137702copy number variation1nstd102humanPathogenic GRCh37 chr9: 35,059,633-37,660,586 , GRCh38.p12 chr9: 35,059,636-37,660,589 TMEM8B, RN7SKP171, 84 more genes
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 RPSAP8, HNRNPA1P26, 275 more genes
    nsv6131470insertion1nstd186human GRCh37 chr19: 41,849,848-41,849,872 , GRCh38.p12 chr19: 41,343,943-41,343,967 TGFB1
    nsv6131464insertion1nstd186human GRCh37 chr17: 64,491,679-64,491,692 , GRCh38.p12 chr17: 66,495,561-66,495,574 PRKCA
    nsv6131381insertion1nstd186human GRCh37 chr15: 51,978,919-51,978,919 , GRCh38.p12 chr15: 51,686,722-51,686,722 SCG3
    nsv6131328mobile element insertion1nstd186human GRCh37 chr1: 169,524,859-169,524,871 , GRCh38.p12 chr1: 169,555,621-169,555,633 F5
    nsv6131202insertion1nstd186human GRCh37 chr19: 54,402,184-54,402,187 , GRCh38.p12 chr19: 53,898,930-53,898,933 PRKCG
    nsv6131079mobile element insertion1nstd186human GRCh37 chr17: 64,637,294-64,637,345 , GRCh38.p12 chr17: 66,641,176-66,641,227 PRKCA
    nsv6130954mobile element insertion1nstd186human GRCh37 chr2: 102,912,432-142,045,768 , GRCh38.p12 chr2: 102,295,972-141,288,199 LINC01106, INSIG2, 623 more genes
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 LOC105369306, LOC107985516, 533 more genes
    nsv6130880insertion1nstd186human GRCh37 chr21: 27,508,495-27,508,509 , GRCh38.p12 chr21: 26,136,177-26,136,191 APP
    nsv6130706insertion1nstd186human GRCh37 chr21: 27,352,122-27,352,185 , GRCh38.p12 chr21: 25,979,809-25,979,872 APP
    nsv6130243insertion1nstd186human GRCh37 chr12: 102,799,045-102,799,080 , GRCh38.p12 chr12: 102,405,267-102,405,302 IGF1, LINC02456
    nsv6130112insertion1nstd186human GRCh37 chr21: 27,252,394-27,252,438 , GRCh38.p12 chr21: 25,880,083-25,880,127 APP
    nsv6129854insertion1nstd186human GRCh37 chr14: 69,417,180-69,417,230 , GRCh38.p12 chr14: 68,950,463-68,950,513 ACTN1
    nsv6129668mobile element insertion1nstd186human GRCh37 chr2: 174,952,231-174,952,282 , GRCh38.p12 chr2: 174,087,503-174,087,554 OLA1
    nsv6128428copy number variation1nstd186human GRCh37 chr18: 52,447,278-52,447,559 , GRCh38.p12 chr18: 54,780,047-54,780,328 RAB27B
    nsv6128229insertion1nstd186human GRCh37 chr5: 148,749,591-148,749,624 , GRCh38.p12 chr5: 149,370,028-149,370,061 PCYOX1L
    nsv6127480copy number variation1nstd186human GRCh37 chr17: 1,654,430-1,655,451 , GRCh38.p12 chr17: 1,751,136-1,752,157 , GRCh38.p12 chr17|NT_187611.1: 180,085-181,106 SERPINF2
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