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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
    nsv5874319copy number variation1nstd209human GRCh38 chrX: 154,400,937-154,401,249 , GRCh37.p13 chrX: 153,629,278-153,629,590 , GRCh37.p13 chrX|NW_003871103.3: 1,834,916-1,835,228 RPL10, DNASE1L1
    nsv5871686copy number variation1nstd209human GRCh38 chrX: 154,402,438-154,402,633 , GRCh37.p13 chrX|NW_003871103.3: 1,836,417-1,836,612 , GRCh37.p13 chrX: 153,630,779-153,630,974 RPL10, DNASE1L1
    nsv5665564copy number variation1nstd207human GRCh38 chrX: 154,402,438-154,402,633 , GRCh37.p13 chrX|NW_003871103.3: 1,836,417-1,836,612 , GRCh37.p13 chrX: 153,630,779-153,630,974 RPL10, DNASE1L1
    nsv5433859copy number variation1nstd206human GRCh38 chrX: 154,400,941-154,401,250 , GRCh37.p13 chrX|NW_003871103.3: 1,834,920-1,835,229 , GRCh37.p13 chrX: 153,629,282-153,629,591 RPL10, DNASE1L1
    nsv5426952copy number variation1nstd206human GRCh38 chrX: 154,402,438-154,402,634 , GRCh37.p13 chrX|NW_003871103.3: 1,836,417-1,836,613 , GRCh37.p13 chrX: 153,630,779-153,630,975 RPL10, DNASE1L1
    nsv5424349copy number variation1nstd206human GRCh38 chrX: 154,394,113-154,396,354 , GRCh37.p13 chrX|NW_003871103.3: 1,828,092-1,830,333 , GRCh37.p13 chrX: 153,622,455-153,624,695 RPL10
    nsv5380362translocation1nstd200human GRCh38 chrX: 154,402,438-154,402,438 , GRCh38 chrX: 154,402,634-154,402,634 , GRCh37.p13 chrX: 153,630,975-153,630,975 , GRCh37.p13 chrX|NW_003871103.3: 1,836,613-1,836,613 , GRCh37.p13 chrX|NW_003871103.3: 1,836,417-1,836,417 , GRCh37.p13 chrX: 153,630,779-153,630,779 DNASE1L1, RPL10
    nsv5380361translocation1nstd200human GRCh38 chrX: 154,401,250-154,401,250 , GRCh38 chrX: 154,400,941-154,400,941 , GRCh37.p13 chrX|NW_003871103.3: 1,834,920-1,834,920 , GRCh37.p13 chrX: 153,629,591-153,629,591 , GRCh37.p13 chrX|NW_003871103.3: 1,835,229-1,835,229 , GRCh37.p13 chrX: 153,629,282-153,629,282 DNASE1L1, RPL10
    nsv5353751translocation1nstd200human GRCh37.p13 chrX|NW_003871103.3: 1,835,372-1,835,372 , GRCh38 chr6: 74,396,988-74,396,988 , GRCh38 chrX: 154,401,393-154,401,393 , GRCh37.p13 chr6: 75,106,704-75,106,704 , GRCh37.p13 chrX: 153,629,734-153,629,734 DNASE1L1, RPL10, 1 more genes
    nsv5338790translocation1nstd200human GRCh37 chrX: 153,630,779-153,630,779 , GRCh37 chrX: 153,630,975-153,630,975 , GRCh38.p12 chrX: 154,402,438-154,402,438 , GRCh38.p12 chrX: 154,402,634-154,402,634 DNASE1L1, RPL10
    nsv5332492translocation1nstd200human GRCh37 chrX: 153,629,282-153,629,282 , GRCh37 chrX: 153,629,591-153,629,591 , GRCh38.p12 chrX: 154,400,941-154,400,941 , GRCh38.p12 chrX: 154,401,250-154,401,250 RPL10, DNASE1L1
    nsv5183633mobile element insertion1nstd203human GRCh37.p13 chrX|NW_003871103.3: 1,833,590-1,833,590 , GRCh38 chrX: 154,399,611-154,399,611 , GRCh37.p13 chrX: 153,627,952-153,627,952 DNASE1L1, RPL10, 1 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
    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
    nsv4754021inversion1nstd199human GRCh37 chrX: 153,564,267-153,624,587 , GRCh38.p12 chrX: 154,335,917-154,396,246 EMD, FLNA, 2 more genes
    nsv4730161inversion20nstd198human GRCh37.p13 chrX: 153,565,303-153,644,627 , GRCh38 chrX: 154,336,953-154,416,288 , GRCh37.p13 chrX|NW_003871103.3: 1,770,932-1,850,267 DNASE1L1, EMD, 5 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
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