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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6836427copy number variation1nstd229human GRCh38 chr7: 127,350,737-127,360,989 , GRCh37.p13 chr7: 126,990,791-127,001,043 ZNF800
    nsv6836217copy number variation1nstd229human GRCh38 chr7: 127,357,391-127,359,130 , GRCh37.p13 chr7: 126,997,445-126,999,184 ZNF800
    nsv6835613copy number variation1nstd229human GRCh38 chr7: 127,259,825-128,156,259 , GRCh37.p13 chr7: 126,899,879-127,796,311 LOC105375489, PRELID3BP10, 13 more genes
    nsv6827460copy number variation1nstd229human GRCh38 chr7: 127,294,769-127,345,539 , GRCh37.p13 chr7: 126,934,823-126,985,593 ZNF800, PRELID3BP10
    nsv6826365copy number variation1nstd229human GRCh38 chr7: 127,356,901-127,367,131 , GRCh37.p13 chr7: 126,996,955-127,007,185 ZNF800
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6561425inversion1nstd223human GRCh38 chr7: 127,340,944-127,341,522 , GRCh37.p13 chr7: 126,980,998-126,981,576 ZNF800
    nsv6435554copy number variation1nstd223human GRCh38 chr7: 127,375,201-127,376,100 , GRCh37.p13 chr7: 127,015,255-127,016,154 ZNF800
    nsv6428458copy number variation1nstd223human GRCh38 chr7: 127,377,497-127,378,011 , GRCh37.p13 chr7: 127,017,551-127,018,065 ZNF800
    nsv6427511copy number variation1nstd223human GRCh38 chr7: 127,391,801-127,393,800 , GRCh37.p13 chr7: 127,031,855-127,033,854 ZNF800
    nsv6427089copy number variation1nstd223human GRCh38 chr7: 127,385,272-127,385,905 , GRCh37.p13 chr7: 127,025,326-127,025,959 ZNF800
    nsv6426950copy number variation1nstd223human GRCh38 chr7: 127,327,601-127,486,000 , GRCh37.p13 chr7: 126,967,655-127,126,054 LINC03012, LOC105375490, 1 more genes
    nsv6419096copy number variation1nstd223human GRCh38 chr7: 127,388,201-127,398,000 , GRCh37.p13 chr7: 127,028,255-127,038,054 ZNF800
    nsv6417340copy number variation1nstd223human GRCh38 chr7: 127,347,601-127,348,300 , GRCh37.p13 chr7: 126,987,655-126,988,354 ZNF800
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
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