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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
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7071284inversion1nstd229human GRCh38 chr15: 82,250,854-84,092,439 , GRCh37.p13 chr15: 82,543,195-84,761,191 HOMER2, EFL1, 46 more genes
    nsv7067903inversion1nstd229human GRCh38 chr15: 82,416,076-84,530,844 , GRCh37.p13 chr15: 82,708,281-85,074,075 RN7SL417P, FABP5P8, 66 more genes
    nsv7065371inversion1nstd229human GRCh38 chr15: 82,262,265-85,274,261 , GRCh37.p13 chr15: 82,554,606-85,817,492 GOLGA6L10, GOLGA6L17P, 96 more genes
    nsv7063845inversion1nstd229human GRCh38 chr15: 82,252,671-83,794,124 , GRCh37.p13 chr15: 82,545,012-84,462,876 CSPG4P10, DNM1P36, 42 more genes
    nsv7063132inversion1nstd229human GRCh38 chr15: 82,261,447-84,086,720 , GRCh37.p13 chr15: 82,553,788-84,755,472 GOLGA6L10, DNM1P38, 46 more genes
    nsv7062974inversion1nstd229human GRCh38 chr15: 82,270,374-84,067,177 , GRCh37.p13 chr15: 82,562,715-84,735,929 BTBD1, LOC105370933, 44 more genes
    nsv7059644inversion1nstd229human GRCh38 chr15: 82,398,536-84,548,330 , GRCh37.p13 chr15: 82,690,748-85,091,561 LOC102724093, CSPG4P11, 66 more genes
    nsv7058879inversion1nstd229human GRCh38 chr15: 82,197,935-85,119,504 , GRCh37.p13 chr15: 82,490,276-85,662,735 LOC103171574, RN7SL417P, 87 more genes
    nsv6969558copy number variation1nstd229human GRCh38 chr15: 83,140,901-83,144,200 , GRCh37.p13 chr15: 83,809,653-83,812,952 TM6SF1, HDGFL3
    nsv6966079copy number variation1nstd229human GRCh38 chr15: 83,082,381-85,945,931 , GRCh37.p13 chr15: 82,808,513-86,489,162 LOC105370936, LOC105370933, 74 more genes
    nsv6960503copy number variation1nstd229human GRCh38 chr15: 83,122,089-83,130,161 , GRCh37.p13 chr15: 83,790,841-83,798,913 TM6SF1, HDGFL3
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6579525inversion1nstd223human GRCh38 chr15: 77,618,608-83,164,280 , GRCh37.p13 chr15: 77,910,950-83,833,032 STARD5, RPL9P8, 131 more genes
    nsv6578911inversion1nstd223human GRCh38 chr15: 77,618,608-84,708,062 , GRCh37.p13 chr15: 77,910,950-85,251,293 TMC3-AS1, LOC642677, 177 more genes
    nsv6577814inversion1nstd223human GRCh38 chr15: 83,143,079-83,143,566 , GRCh37.p13 chr15: 83,811,831-83,812,318 HDGFL3, TM6SF1
    nsv6514316copy number variation1nstd223human GRCh38 chr15: 83,138,301-83,139,900 , GRCh37.p13 chr15: 83,807,053-83,808,652 HDGFL3, TM6SF1
    nsv6501219copy number variation1nstd223human GRCh38 chr15: 83,136,501-83,139,200 , GRCh37.p13 chr15: 83,805,253-83,807,952 TM6SF1, HDGFL3
    nsv6497218copy number variation1nstd223human GRCh38 chr15: 83,122,089-83,130,161 , GRCh37.p13 chr15: 83,790,841-83,798,913 TM6SF1, HDGFL3
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