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Items: 1 to 20 of 326

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 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
    nsv7091498copy number variation1nstd229human GRCh38 chrX: 34,625,128-34,625,334 , GRCh37.p13 chrX: 34,643,245-34,643,451 TMEM47
    nsv7091491copy number variation1nstd229human GRCh38 chrX: 34,570,217-34,629,957 , GRCh37.p13 chrX: 34,588,334-34,648,074 TMEM47
    nsv7091484copy number variation1nstd229human GRCh38 chrX: 34,511,070-34,816,035 , GRCh37.p13 chrX: 34,529,187-34,834,152 TMEM47
    nsv7091481copy number variation1nstd229human GRCh38 chrX: 34,495,993-34,823,838 , GRCh37.p13 chrX: 34,514,110-34,841,955 TMEM47
    nsv7032924inversion1nstd229human GRCh38 chrX: 34,355,734-41,258,887 , GRCh37.p13 chrX: 34,373,851-41,118,140 IMPDH1P2, RPL32P36, 81 more genes
    nsv6636670copy number variation1nstd102humanPathogenic GRCh37 chrX: 32,419,533-37,487,291 , GRCh38.p12 chrX: 32,401,416-37,628,038 FAM47B, FAM47A, 36 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
    nsv6313340copy number variation1nstd102humanUncertain significance GRCh37 chrX: 33,906,163-35,902,937 , GRCh38.p12 chrX: 33,888,046-35,884,820 LOC105373153, SIAH1P1, 12 more genes
    nsv6290590copy number variation1nstd102humannot provided GRCh37 chrX: 34,628,048-37,181,355 , GRCh38.p12 chrX: 34,609,931-37,322,102 CFAP47, FTH1P29, 20 more genes
    nsv6137607copy number variation1nstd213human GRCh37 chrX: 4,160,000-52,130,001 , GRCh38.p12 chrX: 4,241,959-52,386,858 NR0B1, AMELX, 630 more genes
    nsv6137606copy number variation1nstd213human GRCh37 chrX: 2,750,000-52,110,001 , GRCh38.p12 chrX: 2,831,959-52,366,858 NR0B1, AMELX, 653 more genes
    nsv6137605copy number variation1nstd213human GRCh37 chrX: 2,680,000-52,110,001 , GRCh38.p12 chrX: 2,761,959-52,366,858 NR0B1, AMELX, 654 more genes
    nsv6137604copy number variation1nstd213human GRCh37 chrX: 2,670,000-49,230,001 , GRCh38.p12 chrX: 2,751,959-49,347,809 NR0B1, AMELX, 588 more genes
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