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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148115copy number variation1nstd102humanUncertain significance GRCh37 chr15: 49,775,348-51,221,365 , GRCh38.p12 chr15: 49,483,151-50,929,168 RNA5SP395, AHCYP7, 24 more genes
    nsv7076356inversion1nstd229human GRCh38 chr15: 49,451,408-49,451,515 , GRCh37.p13 chr15: 49,743,605-49,743,712 FAM227B, FGF7
    nsv7067773inversion1nstd229human GRCh38 chr15: 49,468,891-49,474,630 , GRCh37.p13 chr15: 49,761,088-49,766,827 FGF7, FAM227B
    nsv7067502inversion1nstd229human GRCh38 chr15: 48,513,881-51,354,383 , GRCh37.p13 chr15: 48,806,078-51,646,580 NDUFAF4P1, MIR4713, 49 more genes
    nsv6975274copy number variation1nstd229human GRCh38 chr15: 49,471,514-49,571,398 , GRCh37.p13 chr15: 49,763,711-49,863,595 FGF7, FAM227B, 1 more genes
    nsv6972270copy number variation1nstd229human GRCh38 chr15: 49,359,301-49,427,400 , GRCh37.p13 chr15: 49,651,498-49,719,597 LOC100420615, FGF7, 2 more genes
    nsv6971965copy number variation1nstd229human GRCh38 chr15: 49,416,338-49,428,379 , GRCh37.p13 chr15: 49,708,535-49,720,576 FAM227B, FGF7
    nsv6967634copy number variation1nstd229human GRCh38 chr15: 49,450,529-49,469,307 , GRCh37.p13 chr15: 49,742,726-49,761,504 FAM227B, FGF7
    nsv6966288copy number variation1nstd229human GRCh38 chr15: 49,296,936-49,446,552 , GRCh37.p13 chr15: 49,589,133-49,738,749 FAM227B, GALK2, 2 more genes
    nsv6963614copy number variation1nstd229human GRCh38 chr15: 49,356,901-49,427,800 , GRCh37.p13 chr15: 49,649,098-49,719,997 FGF7, GALK2, 2 more genes
    nsv6961799copy number variation1nstd229human GRCh38 chr15: 49,457,689-49,466,906 , GRCh37.p13 chr15: 49,749,886-49,759,103 FGF7, FAM227B
    nsv6959801copy number variation1nstd229human GRCh38 chr15: 49,428,601-49,430,900 , GRCh37.p13 chr15: 49,720,798-49,723,097 FGF7, FAM227B
    nsv6958830copy number variation1nstd229human GRCh38 chr15: 49,357,801-49,428,200 , GRCh37.p13 chr15: 49,649,998-49,720,397 FAM227B, GALK2, 2 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623120copy number variation1nstd224human GRCh37 chr15: 49,659,779-49,716,845 , GRCh38.p12 chr15: 49,367,582-49,424,648 FGF7, FAM227B, 1 more genes
    nsv6582207inversion1nstd223human GRCh38 chr15: 49,468,888-49,474,630 , GRCh37.p13 chr15: 49,761,085-49,766,827 FAM227B, FGF7
    nsv6514797copy number variation1nstd223human GRCh38 chr15: 49,467,088-49,467,816 , GRCh37.p13 chr15: 49,759,285-49,760,013 FGF7, FAM227B
    nsv6512707copy number variation1nstd223human GRCh38 chr15: 49,428,113-49,428,585 , GRCh37.p13 chr15: 49,720,310-49,720,782 FAM227B, FGF7
    nsv6512603copy number variation1nstd223human GRCh38 chr15: 49,470,728-49,471,012 , GRCh37.p13 chr15: 49,762,925-49,763,209 FGF7, FAM227B
    nsv6512116copy number variation1nstd223human GRCh38 chr15: 49,442,414-49,443,057 , GRCh37.p13 chr15: 49,734,611-49,735,254 FAM227B, FGF7
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