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Items: 1 to 20 of 223

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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
    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
    nsv7078055inversion1nstd229human GRCh38 chr15: 77,920,728-78,733,176 , GRCh37.p13 chr15: 78,213,070-79,025,518 ADAMTS7P3, PSMA4, 23 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
    nsv7076306inversion1nstd229human GRCh38 chr15: 77,989,063-78,733,939 , GRCh37.p13 chr15: 78,281,405-79,026,281 HYKK, CIB2, 21 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
    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
    nsv7060467inversion1nstd229human GRCh38 chr15: 78,592,768-78,592,900 , GRCh37.p13 chr15: 78,885,110-78,885,242 CHRNA5, CHRNA3
    nsv6974626copy number variation1nstd229human GRCh38 chr15: 78,603,301-78,611,500 , GRCh37.p13 chr15: 78,895,643-78,903,842 CHRNA3
    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
    nsv6968716copy number variation1nstd229human GRCh38 chr15: 78,594,607-78,599,912 , GRCh37.p13 chr15: 78,886,949-78,892,254 CHRNA5, CHRNA3
    nsv6965352copy number variation1nstd229human GRCh38 chr15: 78,612,935-78,630,422 , GRCh37.p13 chr15: 78,905,277-78,922,764 CHRNA3, CHRNB4
    nsv6959315copy number variation1nstd229human GRCh38 chr15: 78,607,439-78,688,202 , GRCh37.p13 chr15: 78,899,781-78,980,544 CHRNB4, RPL18P11, 1 more genes
    nsv6958329copy number variation1nstd229human GRCh38 chr15: 78,504,763-78,603,621 , GRCh37.p13 chr15: 78,797,105-78,895,963 PSMA4, HYKK, 2 more genes
    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
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