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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147453copy number variation1nstd232human GRCh37.p13 chr6: 326,490-326,552 , GRCh38.p12 chr6: 326,490-326,552 DUSP22
    nsv7093358copy number variation1nstd102humanUncertain significance GRCh37 chr6: 160,000-820,000 , GRCh38.p12 chr6: 160,000-820,000 EXOC2, LOC105374873, 7 more genes
    nsv7053468inversion1nstd229human GRCh38 chr6: 285,653-485,550 , GRCh37.p13 chr6: 285,653-485,550 EXOC2, DUSP22, 1 more genes
    nsv7053420inversion1nstd229human GRCh38 chr6: 196,722-448,065 , GRCh37.p13 chr6: 196,722-448,065 IRF4, LOC105374870, 2 more genes
    nsv7052544inversion1nstd229human GRCh38 chr6: 214,414-312,292 , GRCh37.p13 chr6: 214,414-312,292 LOC105374870, DUSP22
    nsv7045681inversion1nstd229human GRCh38 chr6: 316,792-316,857 , GRCh37.p13 chr6: 316,792-316,857 DUSP22
    nsv7044946inversion1nstd229human GRCh38 chr6: 255,384-301,863 , GRCh37.p13 chr6: 255,384-301,863 DUSP22
    nsv7044237inversion1nstd229human GRCh38 chr6: 299,246-471,853 , GRCh37.p13 chr6: 299,246-471,853 IRF4, DUSP22
    nsv7038280inversion1nstd229human GRCh38 chr6: 208,989-447,796 , GRCh37.p13 chr6: 208,989-447,796 IRF4, LOC105374870, 1 more genes
    nsv6793829copy number variation1nstd229human GRCh38 chr6: 304,866-313,411 , GRCh37.p13 chr6: 304,866-313,411 DUSP22
    nsv6792592copy number variation1nstd229human GRCh38 chr6: 249,501-382,500 , GRCh37.p13 chr6: 249,501-382,500 DUSP22
    nsv6783479copy number variation1nstd229human GRCh38 chr6: 288,099-300,085 , GRCh37.p13 chr6: 288,099-300,085 DUSP22
    nsv6781638copy number variation1nstd229human GRCh38 chr6: 343,021-344,233 , GRCh37.p13 chr6: 343,021-344,233 DUSP22
    nsv6778703copy number variation1nstd229human GRCh38 chr6: 340,942-340,994 , GRCh37.p13 chr6: 340,942-340,994 DUSP22
    nsv6636564copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,975-3,718,881 , GRCh38.p12 chr6: 156,975-3,718,647 LOC101927691, LOC107986555, 60 more genes
    nsv6631243copy number variation4nstd224human GRCh37 chr6: 304,637-348,810 , GRCh38.p12 chr6: 304,637-348,810 DUSP22
    nsv6631238copy number variation2nstd224human GRCh37 chr6: 290,438-345,896 , GRCh38.p12 chr6: 290,438-345,896 DUSP22
    nsv6631236copy number variation2nstd224human GRCh37 chr6: 277,262-370,497 , GRCh38.p12 chr6: 277,262-370,497 DUSP22
    nsv6631145copy number variation1nstd224human GRCh37 chr6: 275,561-337,159 , GRCh38.p12 chr6: 275,561-337,159 DUSP22
    nsv6631144copy number variation1nstd224human GRCh37 chr6: 275,561-335,156 , GRCh38.p12 chr6: 275,561-335,156 DUSP22
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