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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148140copy number variation1nstd102humanPathogenic GRCh38 chrX: 23,730,430-32,849,918 , GRCh37.p13 chrX: 23,748,547-32,868,035 ARX, LOC107985632, 85 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098370copy number variation1nstd102humanPathogenic GRCh37 chrX: 28,807,461-33,229,429 , GRCh38.p12 chrX: 28,789,344-33,211,312 FTHL17, LOC100418759, 25 more genes
    nsv7098369copy number variation1nstd102humanPathogenic GRCh37 chrX: 28,807,451-31,241,248 , GRCh38.p12 chrX: 28,789,334-31,223,131 PIGFP3, TAB3-AS1, 19 more genes
    nsv7098019copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 28,807,451-31,201,031 , GRCh38.p12 chrX: 28,789,334-31,182,914 NR0B1, DMD, 19 more genes
    nsv7086876copy number variation1nstd229human GRCh38 chrX: 30,869,874-30,870,073 , GRCh37.p13 chrX: 30,887,991-30,888,190 TAB3
    nsv7086875copy number variation1nstd229human GRCh38 chrX: 30,868,314-30,879,474 , GRCh37.p13 chrX: 30,886,431-30,897,591 TAB3
    nsv7086874copy number variation1nstd229human GRCh38 chrX: 30,847,844-30,848,055 , GRCh37.p13 chrX: 30,865,961-30,866,172 TAB3
    nsv7086873copy number variation1nstd229human GRCh38 chrX: 30,831,761-30,899,631 , GRCh37.p13 chrX: 30,849,878-30,917,748 TAB3, TAB3-AS1
    nsv7086872copy number variation1nstd229human GRCh38 chrX: 30,830,892-30,975,183 , GRCh37.p13 chrX: 30,849,009-30,993,300 TAB3, TAB3-AS1
    nsv7086864copy number variation1nstd229human GRCh38 chrX: 30,740,974-30,831,318 , GRCh37.p13 chrX: 30,759,091-30,849,435 TAB3, LOC100418759
    nsv7086851copy number variation1nstd229human GRCh38 chrX: 30,583,189-30,871,512 , GRCh37.p13 chrX: 30,601,306-30,889,629 GK, LOC100418759, 4 more genes
    nsv7032946inversion1nstd229human GRCh38 chrX: 30,886,109-30,886,186 , GRCh37.p13 chrX: 30,904,226-30,904,303 TAB3
    nsv7022878inversion1nstd229human GRCh38 chrX: 30,860,937-30,860,955 , GRCh37.p13 chrX: 30,879,054-30,879,072 TAB3
    nsv6636148copy number variation1nstd102humanUncertain significance GRCh37 chrX: 30,905,458-31,015,749 , GRCh38.p12 chrX: 30,887,341-30,997,632 TAB3
    nsv6636147copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,879,855-32,902,136 , GRCh38.p12 chrX: 24,861,738-32,884,019 RNA5SP500, MAGEB6, 64 more genes
    nsv6636122copy number variation1nstd102humanPathogenic GRCh37 chrX: 24,675,165-31,490,279 , GRCh38.p12 chrX: 24,657,048-31,472,162 SCARNA23, CKS1BP6, 65 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
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