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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5893876copy number variation1nstd209human GRCh38 chr3: 14,136,680-14,137,355 , GRCh37.p13 chr3: 14,178,180-14,178,855 TMEM43
    nsv5673474copy number variation1nstd102humanPathogenic GRCh37 chr3: 14,166,684-14,220,439 , GRCh38.p12 chr3: 14,125,184-14,178,939 XPC, TMEM43, 3 more genes
    nsv5570342copy number variation1nstd207human GRCh38 chr3: 14,136,680-14,137,355 , GRCh37.p13 chr3: 14,178,180-14,178,855 TMEM43
    nsv5452866copy number variation1nstd206human GRCh38 chr3: 14,140,473-14,140,564 , GRCh37.p13 chr3: 14,181,973-14,182,064 TMEM43
    nsv5434375copy number variation1nstd206human GRCh38 chr3: 14,136,686-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,856 TMEM43
    nsv5388407copy number variation2nstd186human GRCh37 chr3: 14,178,186-14,178,856 , GRCh38.p12 chr3: 14,136,686-14,137,356 TMEM43
    nsv5327466translocation1nstd204human GRCh38.p13 chr3: 14,136,686-14,136,686 , GRCh38.p13 chr3: 14,137,356-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,186 , GRCh37.p13 chr3: 14,178,856-14,178,856 TMEM43
    nsv5205905copy number variation1nstd204human GRCh38.p13 chr3: 14,136,701-14,137,300 , GRCh37.p13 chr3: 14,178,201-14,178,800 TMEM43
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4917903copy number variation1nstd200human GRCh38 chr3: 14,136,686-14,137,356 , GRCh37.p13 chr3: 14,178,186-14,178,856 TMEM43
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796410copy number variation1nstd200human GRCh37 chr3: 14,178,186-14,178,856 , GRCh38.p12 chr3: 14,136,686-14,137,356 TMEM43
    nsv4743117copy number variation1nstd199human GRCh37 chr3: 14,178,176-14,178,853 , GRCh38.p12 chr3: 14,136,676-14,137,353 TMEM43
    nsv4702860copy number variation1nstd195human GRCh37 chr3: 14,178,180-14,178,181 , GRCh38.p12 chr3: 14,136,680-14,136,681 TMEM43
    nsv4681186copy number variation2nstd102humanUncertain significance GRCh37 chr3: 14,166,684-14,183,305 , GRCh38.p12 chr3: 14,125,184-14,141,805 TMEM43, CHCHD4
    nsv4664360copy number variation1nstd186human GRCh37 chr3: 14,178,180-14,178,856 , GRCh38.p12 chr3: 14,136,680-14,137,356 TMEM43
    nsv4659838copy number variation1nstd186human GRCh37 chr3: 14,178,242-14,178,837 , GRCh38.p12 chr3: 14,136,742-14,137,337 TMEM43
    nsv4648760copy number variation1nstd186human GRCh37 chr3: 14,178,054-14,178,856 , GRCh38.p12 chr3: 14,136,554-14,137,356 TMEM43
    nsv4636159copy number variation1nstd186human GRCh37 chr3: 14,178,152-14,178,845 , GRCh38.p12 chr3: 14,136,652-14,137,345 TMEM43
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