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Items: 1 to 20 of 311

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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
    nsv6112670copy number variation1nstd102humanUncertain significance GRCh38 chrX: 77,957,506-78,280,549 , GRCh37.p13 chrX|NW_003871101.3: 514,768-752,267 , GRCh37.p13 chrX: 77,213,003-77,450,502 PGAM4, C4orf46P2, 6 more genes
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5615969insertion1nstd207human GRCh38 chrX: 78,269,606-78,269,606 , GRCh37.p13 chrX: 77,525,103-77,525,103 CYSLTR1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5433345copy number variation1nstd206human GRCh38 chrX: 78,269,061-78,269,589 , GRCh37.p13 chrX: 77,524,558-77,525,086 CYSLTR1
    nsv5428021copy number variation1nstd206human GRCh38 chrX: 78,300,064-78,300,403 , GRCh37.p13 chrX: 77,555,561-77,555,900 CYSLTR1
    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
    nsv4908462copy number variation1nstd200human GRCh38 chrX: 78,289,720-78,290,568 , GRCh37.p13 chrX: 77,545,217-77,546,065 CYSLTR1
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4739269insertion1nstd199human GRCh37 chrX: 77,525,076-77,525,076 , GRCh38.p12 chrX: 78,269,579-78,269,579 CYSLTR1
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 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
    nsv4674818copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,514,079-78,015,580 , GRCh38.p12 chrX: 78,258,582-78,760,083 CYSLTR1, PPATP2, 5 more genes
    nsv4563157mobile element insertion1nstd166human GRCh37.p13 chrX: 77,575,422-77,575,422 , GRCh38.p12 chrX: 78,319,925-78,319,925 CYSLTR1
    nsv4517781copy number variation1nstd166human GRCh37.p13 chrX: 77,108,999-77,658,000 , GRCh38.p12 chrX: 77,853,502-78,402,503 TAF9B, LOC107985669, 9 more genes
    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
    nsv4451868copy number variation1nstd102humanPathogenic GRCh37 chrX: 74,667,077-90,312,981 , GRCh38.p12 chrX: 75,447,242-91,057,982 ZDHHC15, POU3F4, 120 more genes
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