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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
    nsv7087732copy number variation1nstd229human GRCh38 chrX: 46,167,733-46,642,985 , GRCh37.p13 chrX: 46,027,168-46,502,420 LINC01186, SLC9A7, 10 more genes
    nsv7087729copy number variation1nstd229human GRCh38 chrX: 46,142,983-47,749,549 , GRCh37.p13 chrX: 46,002,418-47,608,948 ELK1, LOC100419908, 49 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6636937copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,029,115-46,509,514 , GRCh38.p12 chrX: 46,169,680-46,650,079 PGAM1P7, VEZTP1, 11 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
    nsv6290540copy number variation1nstd102humanUncertain significance GRCh37 chrX: 45,888,817-46,408,619 , GRCh38.p12 chrX: 46,029,382-46,549,184 VEZTP1, ACTBP1, 8 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
    nsv6137389copy number variation1nstd213human GRCh37 chrX: 2,970,000-49,220,001 , GRCh38.p12 chrX: 3,051,959-49,347,809 NR0B1, AMELX, 582 more genes
    nsv6137388copy number variation1nstd213human GRCh37 chrX: 2,680,000-52,120,001 , GRCh38.p12 chrX: 2,761,959-52,376,858 NR0B1, AMELX, 655 more genes
    nsv6137387copy number variation1nstd213human GRCh37 chrX: 2,680,000-49,240,001 , GRCh38.p12 chrX: 2,761,959-49,347,809 NR0B1, AMELX, 588 more genes
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