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Items: 1 to 20 of 346

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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
    nsv7138683copy number variation1nstd232human GRCh37.p13 chr15: 79,084,263-79,084,354 , GRCh38.p12 chr15: 78,791,921-78,792,012 ADAMTS7
    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
    nsv7094636copy number variation1nstd102humanUncertain significance GRCh37 chr15: 78,857,986-81,282,132 , GRCh38.p12 chr15: 78,565,644-80,989,791 LOC646934, RNU6-415P, 51 more genes
    nsv7076420inversion1nstd229human GRCh38 chr15: 77,979,239-78,774,411 , GRCh37.p13 chr15: 78,271,581-79,066,753 CRABP1, IDH3A, 25 more genes
    nsv7074088inversion1nstd229human GRCh38 chr15: 77,979,169-78,774,415 , GRCh37.p13 chr15: 78,271,511-79,066,757 LOC91450, ADAMTS7P3, 25 more genes
    nsv7073482inversion1nstd229human GRCh38 chr15: 77,983,091-78,770,012 , GRCh37.p13 chr15: 78,275,433-79,062,354 LOC646934, CHRNA3, 25 more genes
    nsv7064472inversion1nstd229human GRCh38 chr15: 73,034,378-79,475,825 , GRCh37.p13 chr15: 73,326,719-79,768,167 ANP32BP1, PSTPIP1, 169 more genes
    nsv7063463inversion1nstd229human GRCh38 chr15: 75,234,241-81,337,543 , GRCh37.p13 chr15: 75,526,582-81,629,884 RN7SL327P, LOC105370910, 138 more genes
    nsv7062687inversion1nstd229human GRCh38 chr15: 78,750,079-78,762,793 , GRCh37.p13 chr15: 79,042,421-79,055,135 ADAMTS7, LOC112268143, 1 more genes
    nsv7062066inversion1nstd229human GRCh38 chr15: 77,971,450-78,782,289 , GRCh37.p13 chr15: 78,263,792-79,074,631 CRABP1, LOC105370912, 25 more genes
    nsv7062055inversion1nstd229human GRCh38 chr15: 72,671,162-80,404,440 , GRCh37.p13 chr15: 72,963,503-80,696,782 MIR184, TRK-CTT16-1, 194 more genes
    nsv7059045inversion1nstd229human GRCh38 chr15: 78,762,360-78,774,873 , GRCh37.p13 chr15: 79,054,702-79,067,215 ADAMTS7
    nsv6977324copy number variation1nstd229human GRCh38 chr15: 78,783,887-78,810,989 , GRCh37.p13 chr15: 79,076,229-79,103,331 ADAMTS7
    nsv6975405copy number variation1nstd229human GRCh38 chr15: 78,774,029-78,774,079 , GRCh37.p13 chr15: 79,066,371-79,066,421 ADAMTS7
    nsv6975381copy number variation1nstd229human GRCh38 chr15: 78,748,901-78,758,000 , GRCh37.p13 chr15: 79,041,243-79,050,342 LOC112268143, LOC646938, 1 more genes
    nsv6973275copy number variation1nstd229human GRCh38 chr15: 78,798,786-78,804,213 , GRCh37.p13 chr15: 79,091,128-79,096,555 ADAMTS7
    nsv6970452copy number variation1nstd229human GRCh38 chr15: 78,726,601-78,799,000 , GRCh37.p13 chr15: 79,018,943-79,091,342 ADAMTS7, LOC112268143, 4 more genes
    nsv6969044copy number variation1nstd229human GRCh38 chr15: 77,623,918-81,694,021 , GRCh37.p13 chr15: 77,916,260-81,986,362 ST20-MTHFS, CSPG4P13, 87 more genes
    nsv6968385copy number variation1nstd229human GRCh38 chr15: 78,778,555-78,786,153 , GRCh37.p13 chr15: 79,070,897-79,078,495 ADAMTS7
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