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Items: 1 to 20 of 137

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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
    nsv7098969copy number variation1nstd102humanUncertain significance GRCh37 chr15: 76,518,271-76,566,752 , GRCh38.p12 chr15: 76,225,930-76,274,411 ETFA, TYRO3P
    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
    nsv7094734copy number variation1nstd102humanUncertain significance GRCh37 chr15: 76,508,900-76,603,729 , GRCh38.p12 chr15: 76,216,559-76,311,388 TYRO3P, ETFA
    nsv7075916inversion1nstd229human GRCh38 chr15: 75,241,707-77,965,147 , GRCh37.p13 chr15: 75,534,048-78,257,489 PTPN9, LOC105370902, 60 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 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
    nsv7062257inversion1nstd229human GRCh38 chr15: 75,689,588-77,897,345 , GRCh37.p13 chr15: 75,981,929-78,189,687 KRT8P23, PSTPIP1, 37 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
    nsv7060295inversion1nstd229human GRCh38 chr15: 75,736,549-77,907,855 , GRCh37.p13 chr15: 76,028,890-78,200,197 LOC105370906, RN7SL319P, 36 more genes
    nsv7058318inversion1nstd229human GRCh38 chr15: 75,735,884-77,868,867 , GRCh37.p13 chr15: 76,028,225-78,161,209 UBE2Q2, KRT8P23, 34 more genes
    nsv6976836copy number variation1nstd229human GRCh38 chr15: 76,241,846-76,315,574 , GRCh37.p13 chr15: 76,534,187-76,607,915 TYRO3P, ETFA
    nsv6966277copy number variation1nstd229human GRCh38 chr15: 75,929,054-76,317,441 , GRCh37.p13 chr15: 76,221,395-76,609,782 LOC101929439, ETFA, 4 more genes
    nsv6959835copy number variation1nstd229human GRCh38 chr15: 76,072,101-76,516,700 , GRCh37.p13 chr15: 76,364,442-76,809,041 TYRO3P, ISL2, 5 more genes
    nsv6637828copy number variation1nstd102humanUncertain significance GRCh37 chr15: 76,295,806-76,602,024 , GRCh38.p12 chr15: 76,003,465-76,309,683 NRG4, LOC101929439, 3 more genes
    nsv6637477copy number variation1nstd102humanPathogenic GRCh37 chr15: 74,353,736-77,884,397 , GRCh38.p12 chr15: 74,061,395-77,592,055 PTPN9, NRG4, 96 more genes
    nsv6595525inversion1nstd223human GRCh38 chr15: 75,736,544-77,907,949 , GRCh37.p13 chr15: 76,028,885-78,200,291 ETFA, RN7SL319P, 36 more genes
    nsv6587760inversion1nstd223human GRCh38 chr15: 75,735,470-77,868,880 , GRCh37.p13 chr15: 76,027,811-78,161,222 RN7SKP217, TRK-CTT16-1, 34 more genes
    nsv6582103inversion1nstd223human GRCh38 chr15: 75,332,358-77,947,953 , GRCh37.p13 chr15: 75,624,699-78,240,295 DNM1P9, TSPAN3, 53 more genes
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