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Items: 1 to 20 of 331

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144796copy number variation1nstd232human GRCh37.p13 chrX: 49,454,652-49,454,737 , GRCh38.p12 chrX: 49,690,049-49,690,134 PAGE1
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098786copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-51,241,672 , GRCh38.p12 chrX: 46,606,952-51,498,820 LOC100419232, LOC791091, 172 more genes
    nsv7098319copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chrX: 48,368,209-51,241,672 , GRCh38.p12 chrX: 48,509,821-51,498,820 GRIPAP1, ASMER2, 92 more genes
    nsv7098318copy number variation3nstd102humanUncertain significance GRCh37 chrX: 47,001,716-50,659,607 , GRCh38.p12 chrX: 47,142,317-50,916,607 PYY3, CCDC120, 148 more genes
    nsv7098317copy number variation1nstd102humanPathogenic GRCh37 chrX: 46,466,387-50,659,607 , GRCh38.p12 chrX: 46,606,952-50,916,607 PLP2, RN7SL262P, 160 more genes
    nsv7088066copy number variation1nstd229human GRCh38 chrX: 49,693,701-49,707,500 , GRCh37.p13 chrX: 49,458,304-49,472,103 , GRCh37.p13 chrX|NW_004070880.2: 1,883,130-1,896,929 PAGE1
    nsv7088065copy number variation1nstd229human GRCh38 chrX: 49,665,946-50,406,854 , GRCh37.p13 chrX: 49,430,549-50,149,852 , GRCh37.p13 chrX|NW_004070880.2: 1,855,375-2,418,393 PAGE4, MIR501, 18 more genes
    nsv7088061copy number variation1nstd229human GRCh38 chrX: 49,640,631-49,701,977 , GRCh37.p13 chrX|NW_004070880.2: 1,830,060-1,891,406 , GRCh37.p13 chrX: 49,405,234-49,466,580 PAGE1, SALL1P1
    nsv7028188inversion1nstd229human GRCh38 chrX: 48,271,055-52,545,048 , GRCh37.p13 chrX|NW_004070877.1: 1-2,258,163 SSXP8, CACNA1F, 141 more genes
    nsv6637114copy number variation1nstd102humanUncertain significance GRCh37 chrX: 49,371,149-49,636,439 , GRCh38.p12 chrX: 49,606,546-49,871,836 SALL1P1, GAGE1, 3 more genes
    nsv6637069copy number variation1nstd102humanPathogenic GRCh37 chrX: 39,525,562-52,832,596 , GRCh38.p12 chrX: 39,666,308-52,803,572 LOC100419238, NDP, 312 more genes
    nsv6634312copy number variation1nstd102humanUncertain significance GRCh37 chrX: 49,369,600-50,447,320 , GRCh38.p12 chrX: 49,604,997-50,704,320 MIR500B, USP27X, 22 more genes
    nsv6634296copy number variation1nstd102humanUncertain significance GRCh37 chrX: 49,375,617-52,838,206 , GRCh38.p12 chrX: 49,611,014-52,809,182 LOC791098, MAGED1, 80 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
    nsv6315389copy number variation1nstd102humanPathogenic GRCh37 chrX: 11,522,765-155,233,731 , GRCh38.p12 chrX: 11,504,645-156,004,066 RBMX, LOC100129144, 2042 more genes
    nsv6315331copy number variation4nstd102humanPathogenic GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 PLAC1, PGK1P1, 2154 more genes
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