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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6868474copy number variation1nstd229human GRCh38 chr9: 112,616,823-112,830,604 , GRCh37.p13 chr9: 115,379,103-115,592,884 KIAA1958, SNX30, 1 more genes
    nsv6867841copy number variation1nstd229human GRCh38 chr9: 112,701,001-112,769,000 , GRCh37.p13 chr9: 115,463,281-115,531,280 SNX30, INIP
    nsv6866629copy number variation1nstd229human GRCh38 chr9: 112,701,976-112,702,607 , GRCh37.p13 chr9: 115,464,256-115,464,887 INIP
    nsv6866565copy number variation1nstd229human GRCh38 chr9: 112,716,294-112,718,922 , GRCh37.p13 chr9: 115,478,574-115,481,202 INIP
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6632944copy number variation1nstd224human GRCh37 chr9: 115,404,746-115,585,109 , GRCh38.p12 chr9: 112,642,466-112,822,829 INIP, SNX30, 1 more genes
    nsv6559094inversion1nstd223human GRCh38 chr9: 112,704,846-112,705,319 , GRCh37.p13 chr9: 115,467,126-115,467,599 INIP
    nsv6455411copy number variation1nstd223human GRCh38 chr9: 112,681,970-112,682,805 , GRCh37.p13 chr9: 115,444,250-115,445,085 INIP
    nsv6450012copy number variation1nstd223human GRCh38 chr9: 112,609,218-112,871,619 , GRCh37.p13 chr9: 115,371,498-115,633,899 SNX30, INIP, 1 more genes
    nsv6449610copy number variation1nstd223human GRCh38 chr9: 112,714,284-112,728,178 , GRCh37.p13 chr9: 115,476,564-115,490,458 INIP
    nsv6447013copy number variation1nstd223human GRCh38 chr9: 112,681,823-112,682,652 , GRCh37.p13 chr9: 115,444,103-115,444,932 INIP
    nsv6438394copy number variation1nstd223human GRCh38 chr9: 112,701,976-112,702,604 , GRCh37.p13 chr9: 115,464,256-115,464,884 INIP
    nsv6437580copy number variation1nstd223human GRCh38 chr9: 112,717,401-112,719,000 , GRCh37.p13 chr9: 115,479,681-115,481,280 INIP
    nsv6436778copy number variation1nstd223human GRCh38 chr9: 112,695,468-112,697,821 , GRCh37.p13 chr9: 115,457,748-115,460,101 INIP
    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
    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
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