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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5979315inversion1nstd209human GRCh37.p13 chrX: 72,283,506-72,313,441 , GRCh38 chrX: 73,063,667-73,093,602 , GRCh37.p13 chrX|NW_004070882.1: 752,684-782,619 PABPC1L2A, LOC101928380
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5869101copy number variation1nstd209human GRCh38 chrX: 73,075,949-73,076,047 , GRCh37.p13 chrX|NW_004070882.1: 764,966-765,064 , GRCh37.p13 chrX: 72,295,788-72,295,886 PABPC1L2A
    nsv5666877inversion1nstd207human GRCh37.p13 chrX: 72,215,920-72,307,326 , GRCh38 chrX: 72,996,081-73,087,487 , GRCh37.p13 chrX|NW_004070882.1: 685,098-776,504 PABPC1L2A, PABPC1L2B, 2 more genes
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5547524inversion1nstd206human GRCh38 chrX: 73,005,265-73,078,140 , GRCh37.p13 chrX|NW_004070882.1: 694,282-767,157 , GRCh37.p13 chrX: 72,225,104-72,297,979 PABPC1L2A, PABPC1L2B
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4771448copy number variation1nstd200human GRCh37 chrX: 72,295,791-72,295,887 , GRCh38.p12 chrX: 73,075,952-73,076,048 PABPC1L2A
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4764886inversion1nstd199human GRCh37 chrX: 72,222,211-72,300,490 , GRCh38.p12 chrX: 73,002,372-73,080,651 PABPC1L2A, PABPC1L2B, 2 more genes
    nsv4760563inversion1nstd199human GRCh37 chrX: 72,225,399-72,297,318 , GRCh38.p12 chrX: 73,005,560-73,077,479 PABPC1L2A, PABPC1L2B
    nsv4757377inversion1nstd199human GRCh37 chrX: 72,215,923-72,306,774 , GRCh38.p12 chrX: 72,996,084-73,086,935 PABPC1L2A, PABPC1L2B, 2 more genes
    nsv4730106inversion16nstd198human GRCh37.p13 chrX: 72,192,722-72,300,086 , GRCh38 chrX: 72,972,887-73,080,247 , GRCh37.p13 chrX|NW_004070882.1: 661,904-769,264 PABPC1L2A, PABPC1L2B, 2 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4575274mobile element insertion1nstd166human GRCh37.p13 chrX: 72,295,952-72,295,952 , GRCh38.p12 chrX: 73,076,113-73,076,113 PABPC1L2A
    nsv4452492copy number variation1nstd102humanPathogenic GRCh37 chrX: 58,455,352-155,233,731 , GRCh38.p12 chrX: 58,428,919-156,004,066 RNU6-122P, LOC100421910, 1347 more genes
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