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Items: 1 to 20 of 45084

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv915537copy number variation6nstd71human NCBI36 (hg18) chr22: 48,949,014-49,129,839 , GRCh37 (hg19) chr22: 50,606,887-50,782,973 , GRCh38 (hg38) chr22: 50,168,458-50,344,544 PLXNB2, DENND6B, 8 more genes
    nsv915536copy number variation1nstd71human NCBI36 (hg18) chr22: 48,949,014-49,052,476 , GRCh37 (hg19) chr22: 50,606,887-50,710,349 , GRCh38 (hg38) chr22: 50,168,458-50,271,920 MAPK11, PANX2, 5 more genes
    nsv915535copy number variation2nstd71human NCBI36 (hg18) chr22: 48,949,014-49,027,635 , GRCh37 (hg19) chr22: 50,606,887-50,685,508 , GRCh38 (hg38) chr22: 50,168,458-50,247,079 PANX2, TRABD, 3 more genes
    nsv915534copy number variation1nstd71human NCBI36 (hg18) chr22: 48,949,014-49,018,089 , GRCh37 (hg19) chr22: 50,606,887-50,675,962 , GRCh38 (hg38) chr22: 50,168,458-50,237,533 PANX2, TRABD, 2 more genes
    nsv915533copy number variation1nstd71human NCBI36 (hg18) chr22: 48,949,014-49,006,739 , GRCh37 (hg19) chr22: 50,606,887-50,664,612 , GRCh38 (hg38) chr22: 50,168,458-50,226,183 PANX2, TRABD, 2 more genes
    nsv915532copy number variation2nstd71human NCBI36 (hg18) chr22: 48,943,190-49,160,941 , GRCh37 (hg19) chr22: 50,601,063-50,814,075 , GRCh38 (hg38) chr22: 50,162,634-50,375,646 PLXNB2, DENND6B, 8 more genes
    nsv915531copy number variation1nstd71human NCBI36 (hg18) chr22: 48,943,190-49,039,645 , GRCh37 (hg19) chr22: 50,601,063-50,697,518 , GRCh38 (hg38) chr22: 50,162,634-50,259,089 PANX2, MAPK12, 4 more genes
    nsv915530copy number variation2nstd71human NCBI36 (hg18) chr22: 48,941,593-49,160,941 , GRCh37 (hg19) chr22: 50,599,466-50,814,075 , GRCh38 (hg38) chr22: 50,161,037-50,375,646 PLXNB2, DENND6B, 9 more genes
    nsv915529copy number variation1nstd71human NCBI36 (hg18) chr22: 48,941,593-49,129,839 , GRCh37 (hg19) chr22: 50,599,466-50,782,973 , GRCh38 (hg38) chr22: 50,161,037-50,344,544 PLXNB2, DENND6B, 9 more genes
    nsv915528copy number variation1nstd71human NCBI36 (hg18) chr22: 48,941,593-49,129,839 , GRCh37 (hg19) chr22: 50,599,466-50,782,973 , GRCh38 (hg38) chr22: 50,161,037-50,344,544 PLXNB2, DENND6B, 9 more genes
    nsv915527copy number variation1nstd71human NCBI36 (hg18) chr22: 48,937,969-49,160,941 , GRCh37 (hg19) chr22: 50,595,842-50,814,075 , GRCh38 (hg38) chr22: 50,157,413-50,375,646 PLXNB2, DENND6B, 9 more genes
    nsv915526copy number variation1nstd71human NCBI36 (hg18) chr22: 48,924,017-49,160,941 , GRCh37 (hg19) chr22: 50,581,890-50,814,075 , GRCh38 (hg38) chr22: 50,143,461-50,375,646 PLXNB2, DENND6B, 9 more genes
    nsv915525copy number variation1nstd71human NCBI36 (hg18) chr22: 48,924,017-48,974,632 , GRCh37 (hg19) chr22: 50,581,890-50,632,505 , GRCh38 (hg38) chr22: 50,143,461-50,194,076 MOV10L1, PANX2, 1 more genes
    nsv915524copy number variation1nstd71human NCBI36 (hg18) chr22: 48,917,487-49,160,941 , GRCh37 (hg19) chr22: 50,575,360-50,814,075 , GRCh38 (hg38) chr22: 50,136,931-50,375,646 PLXNB2, DENND6B, 9 more genes
    nsv915523copy number variation1nstd71human NCBI36 (hg18) chr22: 48,822,235-48,872,778 , GRCh37 (hg19) chr22: 50,480,108-50,530,651 , GRCh38 (hg38) chr22: 50,041,679-50,092,222 TTLL8, MLC1, 1 more genes
    nsv915522copy number variation1nstd71human NCBI36 (hg18) chr22: 48,812,643-49,160,941 , GRCh37 (hg19) chr22: 50,470,516-50,814,075 , GRCh38 (hg38) chr22: 50,032,087-50,375,646 TTLL8, MLC1, 11 more genes
    nsv915521copy number variation1nstd71human NCBI36 (hg18) chr22: 48,806,991-48,888,793 , GRCh37 (hg19) chr22: 50,464,864-50,546,666 , GRCh38 (hg38) chr22: 50,026,435-50,108,237 TTLL8, MLC1, 1 more genes
    nsv915520copy number variation1nstd71human NCBI36 (hg18) chr22: 48,777,607-48,816,984 , GRCh37 (hg19) chr22: 50,435,480-50,474,857 , GRCh38 (hg38) chr22: 49,997,051-50,036,428 TTLL8, IL17REL
    nsv915519copy number variation1nstd71human NCBI36 (hg18) chr22: 48,724,828-48,974,632 , GRCh37 (hg19) chr22: 50,338,824-50,632,505 , GRCh38 (hg38) chr22: 49,945,176-50,194,076 MIR6821, TTLL8, 6 more genes
    nsv915518copy number variation1nstd71human NCBI36 (hg18) chr22: 48,724,828-48,872,778 , GRCh37 (hg19) chr22: 50,338,824-50,530,651 , GRCh38 (hg38) chr22: 49,945,176-50,092,222 MIR6821, TTLL8, 4 more genes
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