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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5450128copy number variation1nstd206human GRCh38 chr2: 216,623,686-216,632,071 , GRCh37.p13 chr2: 217,488,409-217,496,794 IGFBP2
    nsv5440771copy number variation1nstd206human GRCh38 chr2: 216,638,873-216,641,845 , GRCh37.p13 chr2: 217,503,596-217,506,568 IGFBP2
    nsv5220189copy number variation1nstd204human GRCh38.p13 chr2: 216,603,759-216,636,778 , GRCh37.p13 chr2: 217,468,482-217,501,501 PSMB3P2, IGFBP2, 1 more genes
    nsv5029880inversion1nstd200human GRCh38 chr2: 213,444,845-219,177,092 , GRCh37.p13 chr2: 214,309,569-220,041,814 , LOC102724861, 122 more genes
    nsv4916829copy number variation1nstd200human GRCh38 chr2: 216,655,785-216,656,539 , GRCh37.p13 chr2: 217,520,508-217,521,262 IGFBP2
    nsv4916828copy number variation1nstd200human GRCh38 chr2: 216,647,678-216,648,829 , GRCh37.p13 chr2: 217,512,401-217,513,552 IGFBP2
    nsv4916827copy number variation1nstd200human GRCh38 chr2: 216,637,879-216,642,030 , GRCh37.p13 chr2: 217,502,602-217,506,753 IGFBP2
    nsv4795937copy number variation1nstd200human GRCh37 chr2: 217,520,508-217,521,262 , GRCh38.p12 chr2: 216,655,785-216,656,539 IGFBP2
    nsv4795936copy number variation1nstd200human GRCh37 chr2: 217,502,602-217,506,753 , GRCh38.p12 chr2: 216,637,879-216,642,030 IGFBP2
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4728446copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 215,122,019-220,397,907 , GRCh38.p12 chr2: 214,257,295-219,533,185 AAMP, ATIC, 139 more genes
    nsv4673965copy number variation1nstd102humanPathogenic GRCh37 chr2: 216,883,237-220,953,003 , GRCh38.p12 chr2: 216,018,514-220,088,282 LOC105373887, STK11IP, 138 more genes
    nsv4662769copy number variation1nstd186human GRCh37 chr2: 217,497,551-217,502,100 , GRCh38.p12 chr2: 216,632,828-216,637,377 IGFBP2
    nsv4583380copy number variation1nstd183human GRCh37 chr2: 217,497,551-217,502,100 , GRCh38.p12 chr2: 216,632,828-216,637,377 IGFBP2
    nsv4519137copy number variation1nstd166human GRCh37.p13 chr2: 217,507,169-217,507,233 , GRCh38.p12 chr2: 216,642,446-216,642,510 IGFBP2
    nsv4436532copy number variation1nstd102humanPathogenic GRCh37 chr2: 188,926,928-225,298,653 , GRCh38.p12 chr2: 188,062,201-224,433,936 MARS2, KRT18P19, 575 more genes
    nsv4435891copy number variation1nstd102humanPathogenic GRCh37 chr2: 210,779,657-239,879,183 , GRCh38.p12 chr2: 209,914,933-238,957,487 XRCC5, LINC01173, 494 more genes
    nsv4316119inversion1nstd166human GRCh37.p13 chr2: 187,130,612-218,396,189 , GRCh38.p12 chr2: 186,265,885-217,531,466 , ACADL, 453 more genes
    nsv4315068inversion1nstd166human GRCh37.p13 chr2: 208,775,197-231,007,646 , GRCh38.p12 chr2: 207,910,473-230,142,930 , BCS1L, 344 more genes
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