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Items: 1 to 20 of 323

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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
    nsv7086820copy number variation1nstd229human GRCh38 chrX: 30,211,719-30,214,308 , GRCh37.p13 chrX: 30,229,836-30,232,425 MAGEB2, LOC107985632
    nsv7086773copy number variation1nstd229human GRCh38 chrX: 29,795,228-30,351,660 , GRCh37.p13 chrX: 29,813,345-30,369,777 LOC100420324, PLCE1P1, 8 more genes
    nsv7086749copy number variation1nstd229human GRCh38 chrX: 29,586,362-30,274,431 , GRCh37.p13 chrX: 29,604,479-30,292,548 LOC100420324, MAGEB2, 6 more genes
    nsv7086722copy number variation1nstd229human GRCh38 chrX: 29,426,798-30,274,771 , GRCh37.p13 chrX: 29,444,915-30,292,888 MAGEB4, PIGFP3, 7 more genes
    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
    nsv6633860copy number variation1nstd224human GRCh37 chrX: 30,203,382-30,558,941 , GRCh38.p12 chrX: 30,185,265-30,540,824 NR0B1, MAGEB1, 6 more genes
    nsv6633859copy number variation1nstd224human GRCh37 chrX: 30,171,861-30,648,723 , GRCh38.p12 chrX: 30,153,744-30,630,606 MAGEB3, MAGEB2, 9 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
    nsv6313168copy number variation1nstd102humanPathogenic GRCh37 chrX: 28,798,276-32,131,619 , GRCh38.p12 chrX: 28,780,159-32,113,502 NR0B1, RNA5SP501, 21 more genes
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