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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
    nsv7086860copy number variation1nstd229human GRCh38 chrX: 30,699,305-30,700,567 , GRCh37.p13 chrX: 30,717,422-30,718,684 GK
    nsv7086859copy number variation1nstd229human GRCh38 chrX: 30,679,738-30,684,156 , GRCh37.p13 chrX: 30,697,855-30,702,273 GK
    nsv7086858copy number variation1nstd229human GRCh38 chrX: 30,677,685-30,680,194 , GRCh37.p13 chrX: 30,695,802-30,698,311 GK
    nsv7086857copy number variation1nstd229human GRCh38 chrX: 30,670,380-30,670,496 , GRCh37.p13 chrX: 30,688,497-30,688,613 GK
    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
    nsv7086845copy number variation1nstd229human GRCh38 chrX: 30,503,082-30,681,058 , GRCh37.p13 chrX: 30,521,199-30,699,175 FTLP2, CKS1BP6, 2 more genes
    nsv7030686inversion1nstd229human GRCh38 chrX: 30,661,710-30,662,923 , GRCh37.p13 chrX: 30,679,827-30,681,040 GK
    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
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
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