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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137736copy number variation1nstd102humanPathogenic GRCh37 chrX: 153,263,517-155,260,560 , GRCh38.p12 chrX: 153,998,066-156,030,895 H2AB3, GDI1, 83 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
    nsv5879606copy number variation1nstd209human GRCh38 chrX: 154,785,855-154,785,957 , GRCh37.p13 chrX|NW_003871103.3: 2,219,834-2,219,936 , GRCh37.p13 chrX: 154,014,130-154,014,232 MPP1
    nsv5878993copy number variation1nstd209human GRCh38 chrX: 154,598,638-155,803,675 , GRCh37.p13 chrX|NW_003871103.3: 2,032,617-3,110,903 , GRCh37.p13 chrX: 153,826,899-154,906,585 MIR1184-2, TMLHE-AS1, 39 more genes
    nsv5872386copy number variation1nstd209human GRCh38 chrX: 154,795,566-154,798,622 , GRCh37.p13 chrX|NW_003871103.3: 2,229,545-2,232,601 , GRCh37.p13 chrX: 154,023,841-154,026,897 MPP1
    nsv5666610copy number variation1nstd207human GRCh37.p13 chrX|NW_003871103.3: 2,214,538-2,214,734 , GRCh38 chrX: 154,780,559-154,780,755 , GRCh37.p13 chrX: 154,008,834-154,009,030 MPP1
    nsv5432993copy number variation1nstd206human GRCh38 chrX: 154,789,048-154,789,120 , GRCh37.p13 chrX: 154,017,323-154,017,395 , GRCh37.p13 chrX|NW_003871103.3: 2,223,027-2,223,099 MPP1
    nsv5428022copy number variation1nstd206human GRCh38 chrX: 154,781,296-154,781,490 , GRCh37.p13 chrX: 154,009,571-154,009,765 , GRCh37.p13 chrX|NW_003871103.3: 2,215,275-2,215,469 MPP1
    nsv5426982copy number variation1nstd206human GRCh38 chrX: 154,780,564-154,780,756 , GRCh37.p13 chrX: 154,008,839-154,009,031 , GRCh37.p13 chrX|NW_003871103.3: 2,214,543-2,214,735 MPP1
    nsv5419639copy number variation1nstd206human GRCh38 chrX: 154,785,860-154,785,958 , GRCh37.p13 chrX|NW_003871103.3: 2,219,839-2,219,937 , GRCh37.p13 chrX: 154,014,135-154,014,233 MPP1
    nsv5380364translocation1nstd200human GRCh38 chrX: 154,780,564-154,780,564 , GRCh38 chrX: 154,780,756-154,780,756 , GRCh37.p13 chrX|NW_003871103.3: 2,214,543-2,214,543 , GRCh37.p13 chrX|NW_003871103.3: 2,214,735-2,214,735 , GRCh37.p13 chrX: 154,008,839-154,008,839 , GRCh37.p13 chrX: 154,009,031-154,009,031 MPP1
    nsv5377299translocation1nstd200human GRCh38 chrX: 154,799,391-154,799,391 , GRCh38 chrX: 154,792,233-154,792,233 , GRCh37.p13 chrX|NW_003871103.3: 2,226,212-2,226,212 , GRCh37.p13 chrX|NW_003871103.3: 2,233,370-2,233,370 , GRCh37.p13 chrX: 154,020,508-154,020,508 , GRCh37.p13 chrX: 154,027,666-154,027,666 MPP1
    nsv5344354translocation1nstd200human GRCh37 chrX: 154,009,031-154,009,031 , GRCh37 chrX: 154,008,839-154,008,839 , GRCh38.p12 chrX: 154,780,564-154,780,564 , GRCh38.p12 chrX: 154,780,756-154,780,756 MPP1
    nsv5342807translocation1nstd200human GRCh37 chrX: 154,014,135-154,014,135 , GRCh37 chrX: 154,014,233-154,014,233 , GRCh38.p12 chrX: 154,785,860-154,785,860 , GRCh38.p12 chrX: 154,785,958-154,785,958 MPP1
    nsv5164712mobile element insertion1nstd203human GRCh38 chrX: 154,787,028-154,787,030 , GRCh37.p13 chrX|NW_003871103.3: 2,221,007-2,221,009 , GRCh37.p13 chrX: 154,015,303-154,015,305 MPP1
    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
    nsv4787993copy number variation1nstd200human GRCh37 chrX: 154,016,825-154,017,294 , GRCh38.p12 chrX: 154,788,550-154,789,019 MPP1
    nsv4782442copy number variation1nstd200human GRCh37 chrX: 154,031,050-154,197,676 , GRCh38.p12 chrX: 154,802,775-154,969,401 MPP1, H2AB1, 7 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
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