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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7046732inversion1nstd229human GRCh38 chr6: 90,564,826-91,015,152 , GRCh37.p13 chr6: 91,274,545-91,724,870 MAP3K7, LOC105377893, 1 more genes
    nsv7044189inversion1nstd229human GRCh38 chr6: 90,550,131-90,550,172 , GRCh37.p13 chr6: 91,259,850-91,259,891 MAP3K7
    nsv7039447inversion1nstd229human GRCh38 chr6: 90,574,357-90,574,422 , GRCh37.p13 chr6: 91,284,076-91,284,141 MAP3K7
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6813344copy number variation1nstd229human GRCh38 chr6: 90,551,201-90,571,000 , GRCh37.p13 chr6: 91,260,920-91,280,719 MAP3K7
    nsv6808164copy number variation1nstd229human GRCh38 chr6: 90,561,901-90,583,800 , GRCh37.p13 chr6: 91,271,620-91,293,519 MAP3K7
    nsv6803904copy number variation1nstd229human GRCh38 chr6: 89,981,169-90,625,783 , GRCh37.p13 chr6: 90,690,888-91,335,502 MAP3K7, LOC105377890, 4 more genes
    nsv6802616copy number variation1nstd229human GRCh38 chr6: 90,062,110-90,584,560 , GRCh37.p13 chr6: 90,771,829-91,294,279 LOC105377891, MAP3K7, 3 more genes
    nsv6799477copy number variation1nstd229human GRCh38 chr6: 90,506,483-90,511,616 , GRCh37.p13 chr6: 91,216,202-91,221,335 MAP3K7
    nsv6799129copy number variation1nstd229human GRCh38 chr6: 90,527,871-90,528,193 , GRCh37.p13 chr6: 91,237,590-91,237,912 MAP3K7
    nsv6798632copy number variation1nstd229human GRCh38 chr6: 90,360,123-91,104,040 , GRCh37.p13 chr6: 91,069,842-91,813,758 MAP3K7, LOC105377893, 1 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6413728copy number variation1nstd223human GRCh38 chr6: 90,514,801-90,515,800 , GRCh37.p13 chr6: 91,224,520-91,225,519 MAP3K7
    nsv6412489copy number variation1nstd223human GRCh38 chr6: 90,527,856-90,528,177 , GRCh37.p13 chr6: 91,237,575-91,237,896 MAP3K7
    nsv6405866copy number variation1nstd223human GRCh38 chr6: 90,517,301-90,518,200 , GRCh37.p13 chr6: 91,227,020-91,227,919 MAP3K7
    nsv6405166copy number variation1nstd223human GRCh38 chr6: 90,517,901-90,518,900 , GRCh37.p13 chr6: 91,227,620-91,228,619 MAP3K7
    nsv6402214copy number variation1nstd223human GRCh38 chr6: 90,522,801-90,523,600 , GRCh37.p13 chr6: 91,232,520-91,233,319 MAP3K7
    nsv6401567copy number variation1nstd223human GRCh38 chr6: 90,547,272-90,547,906 , GRCh37.p13 chr6: 91,256,991-91,257,625 MAP3K7
    nsv6399553copy number variation1nstd223human GRCh38 chr6: 90,581,352-90,582,201 , GRCh37.p13 chr6: 91,291,071-91,291,920 MAP3K7
    nsv6398073copy number variation1nstd223human GRCh38 chr6: 90,571,101-90,573,000 , GRCh37.p13 chr6: 91,280,820-91,282,719 MAP3K7
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