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Items: 1 to 20 of 410

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5973208inversion1nstd209human GRCh37.p13 chrX|NW_004070885.1: 62,887-242,796 , GRCh38 chrX: 103,926,471-104,106,380 , GRCh37.p13 chrX: 103,181,052-103,351,063 H2BW1, H2BW2, 9 more genes
    nsv5971624copy number variation2nstd209human GRCh37.p13 chrX|NW_004070885.1: 176,293-197,685 , GRCh38 chrX: 104,039,877-104,061,269 , GRCh37.p13 chrX: 103,294,444-103,315,834 H2BW2, H2BW3P, 1 more genes
    nsv5669703inversion1nstd207human GRCh37.p13 chrX: 103,243,228-103,304,899 , GRCh38 chrX: 103,988,652-104,050,333 , GRCh37.p13 chrX|NW_004070885.1: 125,068-186,749 H2BW1, H2BW2, 1 more genes
    nsv5665484inversion1nstd207human GRCh37.p13 chrX: 103,209,549-103,327,772 , GRCh38 chrX: 103,954,976-104,083,087 , GRCh37.p13 chrX|NW_004070885.1: 91,392-219,503 H2BW1, H2BW2, 7 more genes
    nsv5559893sequence alteration1nstd206human GRCh37.p13 chrX|NW_004070885.1: 56,234-248,212 , GRCh38 chrX: 103,919,818-104,111,796 , GRCh37.p13 chrX: 103,174,401-103,356,487 H2BW4P, H2BW3P, 11 more genes
    nsv5557397sequence alteration1nstd206human GRCh37.p13 chrX|NW_004070885.1: 125,139-186,519 , GRCh38 chrX: 103,988,723-104,050,103 , GRCh37.p13 chrX: 103,243,299-103,304,669 H2BW1, H2BW2, 1 more genes
    nsv5430478copy number variation1nstd206human GRCh37.p13 chrX|NW_004070885.1: 139,551-187,416 , GRCh38 chrX: 104,003,135-104,051,000 , GRCh37.p13 chrX: 103,257,707-103,305,566 H2BW2, H2BW1, 1 more genes
    nsv5417647copy number variation1nstd206human GRCh38 chrX: 103,920,542-104,082,542 , GRCh37.p13 chrX|NW_004070885.1: 56,958-218,958 , GRCh37.p13 chrX: 103,175,125-103,327,236 H2BW1, LOC107985662, 8 more genes
    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
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4730200inversion32nstd198human GRCh37.p13 chrX: 103,213,041-103,328,676 , GRCh38 chrX: 103,958,468-104,083,991 , GRCh37.p13 chrX|NW_004070885.1: 94,884-220,407 H2BW1, H2BW2, 7 more genes
    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
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 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
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4674555copy number variation1nstd102humanLikely benign GRCh37 chrX: 103,140,138-103,299,515 , GRCh38.p12 chrX: 103,885,217-104,044,947 H2BW4P, TMSB15B, 8 more genes
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