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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071944inversion1nstd229human GRCh38 chr9: 112,837,403-112,934,329 , GRCh37.p13 chr9: 115,599,683-115,696,609 SNX30, SLC46A2
    nsv6876423copy number variation1nstd229human GRCh38 chr9: 112,884,079-112,891,141 , GRCh37.p13 chr9: 115,646,359-115,653,421 SLC46A2
    nsv6874510copy number variation1nstd229human GRCh38 chr9: 112,894,330-112,902,223 , GRCh37.p13 chr9: 115,656,610-115,664,503 SLC46A2
    nsv6872351copy number variation1nstd229human GRCh38 chr9: 112,894,850-112,895,267 , GRCh37.p13 chr9: 115,657,130-115,657,547 SLC46A2
    nsv6860674copy number variation1nstd229human GRCh38 chr9: 112,890,976-112,896,524 , GRCh37.p13 chr9: 115,653,256-115,658,804 SLC46A2
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6561628inversion1nstd223human GRCh38 chr9: 112,893,784-112,894,601 , GRCh37.p13 chr9: 115,656,064-115,656,881 SLC46A2
    nsv6449740copy number variation1nstd223human GRCh38 chr9: 112,894,330-112,902,220 , GRCh37.p13 chr9: 115,656,610-115,664,500 SLC46A2
    nsv6315460copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,673,200-115,935,268 , GRCh38.p12 chr9: 110,910,920-113,172,988 MIR4668, LINC02977, 40 more genes
    nsv6315405copy number variation1nstd102humanUncertain significance GRCh37 chr9: 19,356,861-119,513,311 , GRCh38.p12 chr9: 19,356,863-116,751,032 RNU6-156P, GDA, 1425 more genes
    nsv6314062copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 109,265,628-117,650,999 , GRCh38.p12 chr9: 106,503,347-114,888,719 ALAD, AMBP, 151 more genes
    nsv6313900copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 71,349,994-122,603,410 , GRCh38.p12 chr9: 68,735,078-119,841,132 ABCA1, ALAD, 793 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6302982copy number variation1nstd186human GRCh37 chr9: 115,656,610-115,664,500 , GRCh38.p12 chr9: 112,894,330-112,902,220 , SLC46A2
    nsv6279726insertion1nstd214human GRCh38 chr9: 112,890,776-112,890,776 , GRCh37.p13 chr9: 115,653,056-115,653,056 SLC46A2
    nsv6136642copy number variation1nstd213human GRCh37 chr9: 114,910,000-115,820,001 , GRCh38.p12 chr9: 112,147,720-113,057,721 SLC46A2, RPL32P22, 15 more genes
    nsv6136641copy number variation1nstd213human GRCh37 chr9: 114,760,000-115,820,001 , GRCh38.p12 chr9: 111,997,720-113,057,721 SUSD1, KIAA1958, 17 more genes
    nsv6136357copy number variation1nstd213human GRCh37 chr9: 114,500,000-115,820,001 , GRCh38.p12 chr9: 111,737,720-113,057,721 HSDL2, ZNF883, 22 more genes
    nsv6095287insertion1nstd212human GRCh38 chr9: 112,895,808-112,895,808 , GRCh37.p13 chr9: 115,658,088-115,658,088 , SLC46A2
    nsv5956499insertion1nstd209human GRCh38 chr9: 112,895,773-112,895,773 , GRCh37.p13 chr9: 115,658,053-115,658,053 , SLC46A2
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