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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
    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
    nsv7091823copy number variation1nstd229human GRCh38 chrX: 53,130,099-53,141,366 , GRCh37.p13 chrX|NW_004070877.1: 2,843,214-2,854,481 , GRCh37.p13 chrX: 53,159,281-53,170,548 RNU7-37P, KANTR, 1 more genes
    nsv7091822copy number variation1nstd229human GRCh38 chrX: 53,112,826-53,112,933 , GRCh37.p13 chrX|NW_004070877.1: 2,825,941-2,826,048 , GRCh37.p13 chrX: 53,142,008-53,142,115 KANTR
    nsv7091821copy number variation1nstd229human GRCh38 chrX: 53,112,598-53,115,587 , GRCh37.p13 chrX|NW_004070877.1: 2,825,713-2,828,702 , GRCh37.p13 chrX: 53,141,780-53,144,769 KANTR
    nsv7091820copy number variation1nstd229human GRCh38 chrX: 53,107,623-53,114,600 , GRCh37.p13 chrX|NW_004070877.1: 2,820,738-2,827,715 , GRCh37.p13 chrX: 53,136,805-53,143,782 KANTR
    nsv7091819copy number variation1nstd229human GRCh38 chrX: 53,097,825-53,101,727 , GRCh37.p13 chrX|NW_004070877.1: 2,810,940-2,814,842 , GRCh37.p13 chrX: 53,127,007-53,130,909 KANTR
    nsv7091818copy number variation1nstd229human GRCh38 chrX: 53,085,552-53,101,955 , GRCh37.p13 chrX: 53,114,734-53,131,137 , GRCh37.p13 chrX|NW_004070877.1: 2,798,667-2,815,070 TSPYL2, KANTR
    nsv7030885inversion1nstd229human GRCh38 chrX: 52,934,179-55,490,651 , GRCh37.p13 chrX|NW_004070877.1: 2,647,294-4,110,759 , GRCh37.p13 chrX: 52,963,388-54,424,077 MRPS18CP7, TRO, 58 more genes
    nsv7025488inversion1nstd229human GRCh38 chrX: 53,132,362-53,132,394 , GRCh37.p13 chrX|NW_004070877.1: 2,845,477-2,845,509 , GRCh37.p13 chrX: 53,161,544-53,161,576 KANTR
    nsv7025237inversion1nstd229human GRCh38 chrX: 50,557,525-57,228,328 , GRCh37.p13 chrX|NW_004070877.1: 270,640-4,110,759 , GRCh37.p13 chrX: 50,300,525-54,424,077 UBQLN2, IPO7P1, 141 more genes
    nsv7024973inversion1nstd229human GRCh38 chrX: 52,579,324-53,511,387 , GRCh37.p13 chrX|NW_004070877.1: 2,292,439-3,224,502 , GRCh37.p13 chrX: 52,608,336-53,538,353 LOC107985659, RNU7-37P, 37 more genes
    nsv6637081copy number variation1nstd102humanUncertain significance GRCh37 chrX: 52,923,472-53,289,919 , GRCh38.p12 chrX: 52,894,443-53,260,737 ACTG1P10, FAM156A, 9 more genes
    nsv6635186copy number variation1nstd227human GRCh37 chrX: 52,951,462-53,299,420 , GRCh38.p12 chrX: 52,922,271-53,270,238 ACTG1P10, KDM5C, 8 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
    nsv6315330copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-57,841,304 , GRCh38.p12 chrX: 251,879-57,814,871 NPM1P9, UBE2E4P, 799 more genes
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