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Items: 1 to 20 of 577

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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
    nsv7137210copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-76,085,232 , GRCh38.p12 chr15: 72,650,843-75,792,891 LOC105370892, MRPS15P1, 99 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
    nsv7094733copy number variation1nstd102humanUncertain significance GRCh37 chr15: 75,628,431-76,054,677 , GRCh38.p12 chr15: 75,336,090-75,762,336 LOC101929408, MAN2C1, 16 more genes
    nsv7077484inversion1nstd229human GRCh38 chr15: 74,072,224-75,785,570 , GRCh37.p13 chr15: 74,364,565-76,077,911 LOC107984720, SCAMP2, 68 more genes
    nsv7077374inversion1nstd229human GRCh38 chr15: 74,978,016-75,592,041 , GRCh37.p13 chr15: 75,270,357-75,884,382 PPCDC, RPL13P4, 21 more genes
    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
    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
    nsv7061284inversion1nstd229human GRCh38 chr15: 75,494,371-75,502,540 , GRCh37.p13 chr15: 75,786,712-75,794,881 PTPN9, LOC105370902
    nsv7060181inversion1nstd229human GRCh38 chr15: 75,483,598-75,483,747 , GRCh37.p13 chr15: 75,775,939-75,776,088 LOC105370902, PTPN9
    nsv7059590inversion1nstd229human GRCh38 chr15: 75,219,584-75,775,597 , GRCh37.p13 chr15: 75,511,925-76,067,938 LOC107984720, MIR631, 25 more genes
    nsv6977704copy number variation1nstd229human GRCh38 chr15: 75,497,086-75,501,763 , GRCh37.p13 chr15: 75,789,427-75,794,104 LOC105370902, PTPN9
    nsv6976129copy number variation1nstd229human GRCh38 chr15: 75,339,333-75,474,591 , GRCh37.p13 chr15: 75,631,674-75,766,932 SIN3A, COMMD4, 6 more genes
    nsv6973144copy number variation1nstd229human GRCh38 chr15: 75,529,936-75,545,669 , GRCh37.p13 chr15: 75,822,277-75,838,010 PTPN9
    nsv6973093copy number variation1nstd229human GRCh38 chr15: 75,515,101-75,517,100 , GRCh37.p13 chr15: 75,807,442-75,809,441 PTPN9
    nsv6971691copy number variation1nstd229human GRCh38 chr15: 75,516,315-75,516,427 , GRCh37.p13 chr15: 75,808,656-75,808,768 PTPN9
    nsv6969975copy number variation1nstd229human GRCh38 chr15: 75,559,301-75,564,900 , GRCh37.p13 chr15: 75,851,642-75,857,241 PTPN9
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