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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
    nsv7091817copy number variation1nstd229human GRCh38 chrX: 53,076,869-53,077,561 , GRCh37.p13 chrX|NW_004070877.1: 2,789,984-2,790,676 , GRCh37.p13 chrX: 53,106,051-53,106,743 GPR173
    nsv7091816copy number variation1nstd229human GRCh38 chrX: 53,076,843-53,077,373 , GRCh37.p13 chrX|NW_004070877.1: 2,789,958-2,790,488 , GRCh37.p13 chrX: 53,106,025-53,106,555 GPR173
    nsv7091815copy number variation1nstd229human GRCh38 chrX: 53,065,273-53,067,362 , GRCh37.p13 chrX|NW_004070877.1: 2,778,388-2,780,477 , GRCh37.p13 chrX: 53,094,455-53,096,544 GPR173
    nsv7091814copy number variation1nstd229human GRCh38 chrX: 53,063,301-53,066,400 , GRCh37.p13 chrX|NW_004070877.1: 2,776,416-2,779,515 , GRCh37.p13 chrX: 53,092,483-53,095,582 GPR173
    nsv7091813copy number variation1nstd229human GRCh38 chrX: 53,063,230-53,066,441 , GRCh37.p13 chrX|NW_004070877.1: 2,776,345-2,779,556 , GRCh37.p13 chrX: 53,092,412-53,095,623 GPR173
    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
    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
    nsv6315228copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,104,986-54,034,505 , GRCh38.p12 chrX: 53,075,804-54,008,072 TIPINP1, MIRLET7F2, 21 more genes
    nsv6313227copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 52,881,435-55,684,871 , GRCh38.p12 chrX: 52,852,398-55,658,438 ACTG1P10, ALAS2, 64 more genes
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