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Items: 1 to 20 of 494

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098606copy number variation1nstd102humanPathogenic GRCh37 chrX: 17,393,881-18,525,300 , GRCh38.p12 chrX: 17,375,758-18,507,180 BEND2, FAM136GP, 13 more genes
    nsv7098357copy number variation1nstd102humanUncertain significance GRCh37 chrX: 17,393,881-18,665,472 , GRCh38.p12 chrX: 17,375,758-18,647,352 MDM4P1, RS1, 15 more genes
    nsv7085978copy number variation1nstd229human GRCh38 chrX: 18,353,726-18,354,151 , GRCh37.p13 chrX: 18,371,846-18,372,271 SCML2
    nsv7085977copy number variation1nstd229human GRCh38 chrX: 18,341,582-18,345,941 , GRCh37.p13 chrX: 18,359,702-18,364,061 TMSB10P2, SCML2
    nsv7085976copy number variation1nstd229human GRCh38 chrX: 18,260,601-18,262,000 , GRCh37.p13 chrX: 18,278,721-18,280,120 SCML2
    nsv7085910copy number variation1nstd229human GRCh38 chrX: 17,506,256-19,477,473 , GRCh37.p13 chrX: 17,524,379-19,495,591 TRV-TAC1-2, LOC101928389, 26 more genes
    nsv7085539copy number variation1nstd229human GRCh38 chrX: 15,461,305-24,177,792 , GRCh37.p13 chrX: 15,479,428-24,195,909 LOC105373146, PIR-FIGF, 104 more genes
    nsv7037348inversion1nstd229human GRCh38 chrX: 18,264,473-18,264,502 , GRCh37.p13 chrX: 18,282,593-18,282,622 SCML2
    nsv7037021inversion1nstd229human GRCh38 chrX: 14,941,162-18,599,007 , GRCh37.p13 chrX: 14,959,284-18,617,127 TXLNG, MIR4768, 54 more genes
    nsv7021157inversion1nstd229human GRCh38 chrX: 14,244,684-19,508,867 , GRCh37.p13 chrX: 14,262,806-19,526,985 CA5BP1, CDKL5, 74 more genes
    nsv6636132copy number variation1nstd102humanUncertain significance GRCh37 chrX: 17,751,088-18,863,732 , GRCh38.p12 chrX: 17,732,968-18,845,614 SCML2, RS1, 15 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634135copy number variation1nstd224human GRCh37 chrX: 2,700,157-26,836,730 , GRCh38.p12 chrX: 2,782,116-26,818,613 AMELX, ARSF, 258 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
    nsv6290503copy number variation1nstd102humanUncertain significance GRCh37 chrX: 17,668,096-18,275,579 , GRCh38.p12 chrX: 17,649,976-18,257,459 FAM136GP, BEND2, 7 more genes
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