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Items: 1 to 20 of 319

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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
    nsv7080891copy number variation1nstd229human GRCh38 chrX: 39,384,662-39,388,325 , GRCh37.p13 chrX: 39,243,916-39,247,579 LOC105373176, LINC01282
    nsv7080890copy number variation1nstd229human GRCh38 chrX: 39,381,641-39,403,382 , GRCh37.p13 chrX: 39,240,895-39,262,636 LINC01282, LINC01283, 1 more genes
    nsv7080889copy number variation1nstd229human GRCh38 chrX: 39,375,279-39,375,316 , GRCh37.p13 chrX: 39,234,533-39,234,570 LINC01282
    nsv7080888copy number variation1nstd229human GRCh38 chrX: 39,373,547-40,258,854 , GRCh37.p13 chrX: 39,232,801-40,118,107 LOC107985687, LOC105373178, 11 more genes
    nsv7080887copy number variation1nstd229human GRCh38 chrX: 39,369,167-39,380,900 , GRCh37.p13 chrX: 39,228,421-39,240,154 LINC01282
    nsv7080833copy number variation1nstd229human GRCh38 chrX: 38,929,646-39,785,964 , GRCh37.p13 chrX: 38,788,900-39,645,218 LOC105373175, LOC105373178, 9 more genes
    nsv7036632inversion1nstd229human GRCh38 chrX: 38,929,527-39,411,161 , GRCh37.p13 chrX: 38,788,781-39,270,415 LINC01281, LINC01282, 4 more genes
    nsv7033650inversion1nstd229human GRCh38 chrX: 37,770,465-43,935,549 , GRCh37.p13 chrX: 37,669,767-43,794,795 RN7SL15P, NANOGP10, 79 more genes
    nsv7032924inversion1nstd229human GRCh38 chrX: 34,355,734-41,258,887 , GRCh37.p13 chrX: 34,373,851-41,118,140 IMPDH1P2, RPL32P36, 81 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
    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
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