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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4398336copy number variation1nstd174human GRCh37 chr1: 214,778,841-214,782,576 , GRCh38.p12 chr1: 214,605,498-214,609,233 CENPF, ABHD17AP3
    nsv4359585copy number variation1nstd102humanPathogenic NCBI36 chr1: 207,886,175-247,191,935 , GRCh37.p13 chr1: 209,819,552-249,225,312 , GRCh38.p12 chr1: 209,646,207-248,931,113 CENPF, ACTN2, 784 more genes
    nsv4357949copy number variation1nstd102humanPathogenic NCBI36 chr1: 185,379,736-222,553,742 , GRCh37.p13 chr1: 187,113,113-224,487,119 , GRCh38.p12 chr1: 187,143,981-224,299,417 CENPF, ATF3, 610 more genes
    nsv4356980copy number variation1nstd102humanPathogenic NCBI36 chr1: 212,263,778-247,179,291 , GRCh37.p13 chr1: 214,197,155-249,212,668 , GRCh38.p12 chr1: 214,023,812-248,918,469 CENPF, ACTN2, 704 more genes
    nsv4355874copy number variation1nstd102humanPathogenic NCBI36 chr1: 208,203,593-247,179,291 , GRCh37.p13 chr1: 210,136,970-249,212,668 , GRCh38.p12 chr1: 209,963,625-248,918,469 CENPF, ACTN2, 775 more genes
    nsv4351639copy number variation1nstd102humanUncertain significance NCBI36 chr1: 212,263,778-214,838,138 , GRCh37.p13 chr1: 214,197,155-216,771,515 , GRCh38.p12 chr1: 214,023,812-216,598,173 CENPF, USH2A, 21 more genes
    nsv4346772copy number variation1nstd102humanUncertain significance GRCh37 chr1: 214,201,917-217,501,133 , GRCh38.p12 chr1: 214,028,574-217,327,791 CENPF, KCTD3, 23 more genes
    nsv4346771copy number variation1nstd102humanPathogenic GRCh37 chr1: 207,519,987-249,224,684 , GRCh38.p12 chr1: 207,346,642-248,930,485 CENPF, AGT, 829 more genes
    nsv4346519copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,734,042-225,596,400 , GRCh38.p12 chr1: 204,764,914-225,408,698 CENPF, LOC107985461, 369 more genes
    nsv4327068mobile element insertion1nstd166human GRCh37.p13 chr1: 101,023,630-223,491,166 , GRCh38.p12 chr1: 100,558,074-223,317,824 CENPF, ABL2, 2334 more genes
    nsv4327009mobile element insertion1nstd166human GRCh37.p13 chr1: 214,802,724-214,802,920 , GRCh38.p12 chr1: 214,629,381-214,629,577 CENPF
    nsv4290849insertion1nstd166human GRCh37.p13 chr1: 18,331,489-218,444,393 , GRCh38.p12 chr1: 18,004,995-218,271,051 CENPF, ABCA4, 3887 more genes
    nsv4282682insertion1nstd166human GRCh37.p13 chr1: 103,054,486-230,982,868 , GRCh38.p12 chr1: 102,588,930-230,847,122 CENPF, ACTA1, 2514 more genes
    nsv4278528insertion1nstd166human GRCh37.p13 chr1: 714,059-224,180,377 , GRCh38.p12 chr1: 778,679-223,992,675 CENPF, ADAR, 4499 more genes
    nsv4276497insertion1nstd166human GRCh37.p13 chr1: 102,240,167-245,304,315 , GRCh38.p12 chr1: 101,774,611-245,141,013 CENPF, ADORA1, 2769 more genes
    nsv4276075insertion1nstd166human GRCh37.p13 chr1: 14,307,584-248,376,845 , GRCh38.p12 chr1: 13,981,089-248,213,543 CENPF, ADORA1, 4635 more genes
    nsv4274822insertion1nstd166human GRCh37.p13 chr1: 21,624,331-231,303,388 , GRCh38.p12 chr1: 21,297,838-231,167,642 CENPF, ACTA1, 4114 more genes
    nsv4272468insertion1nstd166human GRCh37.p13 chr1: 9,037,785-221,697,659 , GRCh38.p12 chr1: 8,977,726-221,524,317 CENPF, ACADM, 4214 more genes
    nsv4070390copy number variation1nstd166human GRCh37.p13 chr1: 214,789,606-214,791,893 , GRCh38.p12 chr1: 214,616,263-214,618,550 CENPF
    nsv4067752copy number variation1nstd166human GRCh37.p13 chr1: 214,814,942-214,815,023 , GRCh38.p12 chr1: 214,641,599-214,641,680 CENPF
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