U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 453

    loading data ...

    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
    nsv5975247copy number variation1nstd209human GRCh38 chrX: 77,866,265-77,868,364 , GRCh37.p13 chrX|NW_003871101.3: 423,527-425,626 , GRCh37.p13 chrX: 77,121,762-77,123,861 MAGT1
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5879036copy number variation1nstd209human GRCh38 chrX: 77,865,888-77,868,368 , GRCh37.p13 chrX|NW_003871101.3: 423,150-425,630 , GRCh37.p13 chrX: 77,121,385-77,123,865 MAGT1
    nsv5715522mobile element insertion2nstd211human GRCh38 chrX: 77,853,784-77,853,784 , GRCh37.p13 chrX|NW_003871101.3: 411,046-411,046 , GRCh37.p13 chrX: 77,109,281-77,109,281 MAGT1
    nsv5669464copy number variation1nstd207human GRCh38 chrX: 77,865,888-77,868,368 , GRCh37.p13 chrX|NW_003871101.3: 423,150-425,630 , GRCh37.p13 chrX: 77,121,385-77,123,865 MAGT1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5556710mobile element insertion1nstd206human GRCh38 chrX: 77,853,784-77,853,835 , GRCh37.p13 chrX: 77,109,281-77,109,332 , GRCh37.p13 chrX|NW_003871101.3: 411,046-411,097 MAGT1
    nsv5422154copy number variation1nstd206human GRCh38 chrX: 77,789,755-77,890,002 , GRCh37.p13 chrX|NW_003871101.3: 347,017-447,264 , GRCh37.p13 chrX: 77,045,234-77,145,499 MAGT1, RNU6-854P, 1 more genes
    nsv5421041copy number variation1nstd206human GRCh38 chrX: 77,832,226-77,832,513 , GRCh37.p13 chrX|NW_003871101.3: 389,488-389,775 , GRCh37.p13 chrX: 77,087,723-77,088,010 MAGT1
    nsv5385061copy number variation1nstd186human GRCh37 chrX: 77,121,472-77,123,851 , GRCh38.p12 chrX: 77,865,975-77,868,354 MAGT1
    nsv5381755copy number variation1nstd102humanUncertain significance GRCh37 chrX: 77,084,717-77,131,114 , GRCh38.p12 chrX: 77,829,220-77,875,617 MAGT1, RNU6-854P
    nsv5376540translocation1nstd200human GRCh38 chrX: 77,890,002-77,890,002 , GRCh38 chrX: 77,789,755-77,789,755 , GRCh37.p13 chrX: 77,145,499-77,145,499 , GRCh37.p13 chrX|NW_003871101.3: 447,264-447,264 , GRCh37.p13 chrX|NW_003871101.3: 347,017-347,017 , GRCh37.p13 chrX: 77,045,234-77,045,234 MAGT1
    nsv5182106mobile element insertion1nstd203human GRCh38 chrX: 77,853,766-77,853,784 , GRCh37.p13 chrX|NW_003871101.3: 411,028-411,046 , GRCh37.p13 chrX: 77,109,263-77,109,281 MAGT1
    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
    nsv4908457copy number variation1nstd200human GRCh38 chrX: 77,865,920-77,868,407 , GRCh37.p13 chrX: 77,121,417-77,123,904 , GRCh37.p13 chrX|NW_003871101.3: 423,182-425,669 MAGT1
    nsv4908456copy number variation1nstd200human GRCh38 chrX: 77,831,205-77,834,501 , GRCh37.p13 chrX|NW_003871101.3: 388,467-391,763 , GRCh37.p13 chrX: 77,086,702-77,089,998 MAGT1
    nsv4782126copy number variation1nstd200human GRCh37 chrX: 77,003,876-77,148,502 , GRCh38.p12 chrX: 77,748,395-77,893,005 RNU6-854P, RN7SL460P, 2 more genes
    nsv4771564copy number variation1nstd200human GRCh37 chrX: 77,129,721-77,130,689 , GRCh38.p12 chrX: 77,874,224-77,875,192 MAGT1
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center