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Items: 1 to 20 of 611

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116766copy number variation1nstd186human GRCh37 chr6: 170,707,499-170,708,958 , GRCh38.p12 chr6: 170,398,411-170,399,870 , GRCh38.p12 chr6|NT_187553.1: 134,972-136,431 FAM120B
    nsv5976105inversion1nstd209human GRCh38 chr6: 170,264,882-170,388,789 , GRCh37.p13 chr6: 170,573,970-170,697,877 DLL1, FAM120B, 3 more genes
    nsv5950259insertion1nstd209human GRCh38 chr6: 170,407,727-170,407,727 , GRCh37.p13 chr6: 170,716,815-170,716,815 FAM120B
    nsv5922991copy number variation1nstd209human GRCh38 chr6: 170,368,995-170,369,126 , GRCh37.p13 chr6: 170,678,083-170,678,214 FAM120B
    nsv5908858copy number variation1nstd209human GRCh38 chr6: 170,343,273-170,344,477 , GRCh37.p13 chr6: 170,652,361-170,653,565 FAM120B
    nsv5644526insertion1nstd207human GRCh38 chr6: 170,376,968-170,376,968 , GRCh37.p13 chr6: 170,686,056-170,686,056 FAM120B
    nsv5643678insertion1nstd207human GRCh38 chr6: 170,377,663-170,377,663 , GRCh37.p13 chr6: 170,686,751-170,686,751 FAM120B
    nsv5643198insertion1nstd207human GRCh38 chr6: 170,327,662-170,327,662 , GRCh37.p13 chr6: 170,636,750-170,636,750 FAM120B
    nsv5643179insertion1nstd207human GRCh38 chr6: 170,377,326-170,377,326 , GRCh37.p13 chr6: 170,686,414-170,686,414 FAM120B
    nsv5637892insertion2nstd207human GRCh38 chr6: 170,398,809-170,398,809 , GRCh37.p13 chr6: 170,707,897-170,707,897 FAM120B
    nsv5637688insertion1nstd207human GRCh38 chr6: 170,399,170-170,399,170 , GRCh37.p13 chr6: 170,708,258-170,708,258 FAM120B
    nsv5637572insertion1nstd207human GRCh38 chr6: 170,399,817-170,399,817 , GRCh37.p13 chr6: 170,708,905-170,708,905 FAM120B
    nsv5637323insertion1nstd207human GRCh38 chr6: 170,398,670-170,398,670 , GRCh37.p13 chr6: 170,707,758-170,707,758 FAM120B
    nsv5636582insertion1nstd207human GRCh38 chr6: 170,399,173-170,399,173 , GRCh37.p13 chr6: 170,708,261-170,708,261 FAM120B
    nsv5635065insertion2nstd207human GRCh38 chr6: 170,377,196-170,377,196 , GRCh37.p13 chr6: 170,686,284-170,686,284 FAM120B
    nsv5633456insertion1nstd207human GRCh38 chr6: 170,377,447-170,377,447 , GRCh37.p13 chr6: 170,686,535-170,686,535 FAM120B
    nsv5632241insertion1nstd207human GRCh38 chr6: 170,377,914-170,377,914 , GRCh37.p13 chr6: 170,687,002-170,687,002 FAM120B
    nsv5631281insertion1nstd207human GRCh38 chr6: 170,377,012-170,377,012 , GRCh37.p13 chr6: 170,686,100-170,686,100 FAM120B
    nsv5630936insertion1nstd207human GRCh38 chr6: 170,398,770-170,398,770 , GRCh37.p13 chr6: 170,707,858-170,707,858 FAM120B
    nsv5630430insertion3nstd207human GRCh38 chr6: 170,399,483-170,399,483 , GRCh37.p13 chr6: 170,708,571-170,708,571 FAM120B
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