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Items: 1 to 20 of 1233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137813insertion1nstd102humanBenign GRCh37 chr7: 288,155-288,155 , GRCh38 chr7: 248,189-248,189 FAM20C
    nsv6118025copy number variation1nstd186human GRCh37 chr7: 223,978-225,976 , GRCh38.p12 chr7: 223,978-225,976 FAM20C
    nsv5967152insertion1nstd209human GRCh38 chr7: 251,229-251,229 , GRCh37.p13 chr7: 291,195-291,195 FAM20C
    nsv5961673insertion1nstd209human GRCh38 chr7: 217,386-217,386 , GRCh37.p13 chr7: 217,386-217,386 FAM20C
    nsv5959365insertion1nstd209human GRCh38 chr7: 253,609-253,609 , GRCh37.p13 chr7: 293,575-293,575 FAM20C
    nsv5927249copy number variation1nstd209human GRCh38 chr7: 221,019-221,960 , GRCh37.p13 chr7: 221,019-221,960 FAM20C
    nsv5926742copy number variation1nstd209human GRCh38 chr7: 224,015-225,974 , GRCh37.p13 chr7: 224,015-225,974 FAM20C
    nsv5926089copy number variation1nstd209human GRCh38 chr7: 248,177-248,244 , GRCh37.p13 chr7: 288,143-288,210 FAM20C
    nsv5925402copy number variation1nstd209human GRCh38 chr7: 231,383-231,537 , GRCh37.p13 chr7: 231,383-231,537 FAM20C
    nsv5924911copy number variation1nstd209human GRCh38 chr7: 257,728-258,017 , GRCh37.p13 chr7: 297,694-297,983 FAM20C
    nsv5924617copy number variation1nstd209human GRCh38 chr7: 251,143-251,208 , GRCh37.p13 chr7: 291,109-291,174 FAM20C
    nsv5917951copy number variation1nstd209human GRCh38 chr7: 235,078-235,149 , GRCh37.p13 chr: NaN-NaN FAM20C
    nsv5917502copy number variation1nstd209human GRCh38 chr7: 224,043-224,101 , GRCh37.p13 chr7: 224,043-224,101 FAM20C
    nsv5917031copy number variation1nstd209human GRCh38 chr7: 246,147-246,224 , GRCh37.p13 chr7: 286,113-286,190 FAM20C
    nsv5915154copy number variation1nstd209human GRCh37.p13 chr7: 84,361-315,646 , GRCh38 chr7: 84,361-275,680 FAM20C, LINC03014, 4 more genes
    nsv5913554copy number variation1nstd209human GRCh38 chr7: 259,492-259,553 , GRCh37.p13 chr7: 299,458-299,519 FAM20C
    nsv5913428copy number variation1nstd209human GRCh38 chr7: 226,511-226,658 , GRCh37.p13 chr7: 226,511-226,658 FAM20C
    nsv5913250copy number variation1nstd209human GRCh38 chr7: 206,512-206,709 , GRCh37.p13 chr7: 206,512-206,709 FAM20C
    nsv5911725copy number variation1nstd209human GRCh38 chr7: 246,117-246,194 , GRCh37.p13 chr7: 286,083-286,160 FAM20C
    nsv5909695copy number variation1nstd209human GRCh38 chr7: 257,868-258,120 , GRCh37.p13 chr7: 297,834-298,086 FAM20C
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