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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7093157complex substitution1nstd102humanUncertain significance GRCh37.p13 chrX: 103,118,514-103,313,590 , GRCh38 chrX: 103,734,669-104,059,025 , GRCh37.p13 chrX|NW_004070885.1: 1-195,441 PLP1, RAB9B, 13 more genes
    nsv7090650copy number variation1nstd229human GRCh38 chrX: 103,778,715-103,993,486 , GRCh37.p13 chrX: 103,118,514-103,248,054 , GRCh37.p13 chrX|NW_004070885.1: 1-129,902 TMSB15B, H2BW4P, 9 more genes
    nsv7056502inversion1nstd229human GRCh38 chrX: 103,955,056-104,169,610 , GRCh37.p13 chrX|NW_004070885.1: 91,472-306,026 , GRCh37.p13 chrX: 103,209,629-103,414,291 H2BW4P, SLC25A53, 11 more genes
    nsv7052848inversion1nstd229human GRCh37.p13 chrX|NW_004070885.1: 85,284-228,197 , GRCh38 chrX: 103,948,868-104,091,781 , GRCh37.p13 chrX: 103,203,442-103,336,465 DPPA3P4, DPPA3P1, 7 more genes
    nsv7052621inversion1nstd229human GRCh38 chrX: 103,826,879-110,334,422 , GRCh37.p13 chrX: 103,081,809-109,577,650 CSGALNACT2P2, LOC107985662, 82 more genes
    nsv7043972inversion1nstd229human GRCh38 chrX: 103,934,637-103,989,323 , GRCh37.p13 chrX|NW_004070885.1: 71,053-125,739 , GRCh37.p13 chrX: 103,189,211-103,243,897 DPPA3P1, LOC107987334, 2 more genes
    nsv7041038inversion1nstd229human GRCh37.p13 chrX|NW_004070885.1: 87,364-227,304 , GRCh38 chrX: 103,950,948-104,090,888 , GRCh37.p13 chrX: 103,205,522-103,335,572 H2BW1, TMSB15B, 7 more genes
    nsv7038256inversion1nstd229human GRCh38 chrX: 103,921,291-104,110,334 , GRCh37.p13 chrX: 103,175,874-103,355,025 , GRCh37.p13 chrX|NW_004070885.1: 57,707-246,750 SLC25A53, H2BW4P, 9 more genes
    nsv6636543copy number variation1nstd102humanPathogenic GRCh37 chrX: 93,805,850-118,913,329 , GRCh38.p12 chrX: 94,550,851-119,779,366 TRPC5OS, LOC105373314, 351 more genes
    nsv6636471copy number variation1nstd102humanPathogenic GRCh37 chrX: 103,017,429-103,236,332 , GRCh38.p12 chrX: 103,762,501-103,981,754 DPPA3P1, TMSB15B-AS1, 9 more genes
    nsv6634623copy number variation1nstd102humanPathogenic GRCh38 chrX: 103,776,506-104,817,980 , GRCh37.p13 chrX: 103,031,434-104,062,660 SLC25A53P1, ELF2P1, 22 more genes
    nsv6634595copy number variation1nstd102humanPathogenic GRCh38 chrX: 103,477,300-104,817,980 , GRCh37.p13 chrX: 102,732,228-104,062,660 TMSB15B, MORF4L2-AS1, 33 more genes
    nsv6634329copy number variation1nstd102humanPathogenic GRCh37 chrX: 76,794,355-119,282,836 , GRCh38.p12 chrX: 77,538,874-120,148,930 NXF4, RHOXF1P1, 489 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634037copy number variation2nstd224human GRCh37 chrX: 103,200,296-103,349,129 , GRCh38.p12 chrX: 103,945,722-104,104,446 H2BW4P, H2BW3P, 8 more genes
    nsv6634036copy number variation2nstd224human GRCh37 chrX: 103,200,296-103,295,458 , GRCh38.p12 chrX: 103,945,722-104,040,891 H2BW1, H2BW2, 4 more genes
    nsv6633953copy number variation2nstd224human GRCh37 chrX: 103,221,144-103,349,129 , GRCh38.p12 chrX: 103,966,571-104,104,446 H2BW1, H2BW2, 7 more genes
    nsv6633952copy number variation10nstd224human GRCh37 chrX: 103,200,296-103,301,842 , GRCh38.p12 chrX: 103,945,722-104,047,274 H2BW1, H2BW2, 4 more genes
    nsv6633744copy number variation1nstd224human GRCh37 chrX: 103,210,117-103,349,156 , GRCh38.p12 chrX: 103,955,544-104,104,473 H2BW1, LOC107985662, 8 more genes
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