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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3917197copy number variation1nstd102humanLikely benign GRCh38 chr15: 94,324,551-94,470,012 , NCBI36 chr15: 92,668,784-92,814,245 , GRCh37 chr15: 94,867,780-95,013,241 MCTP2
    nsv3896818copy number variation1nstd102humanBenign GRCh37 chr15: 94,884,980-94,888,275 , GRCh38.p12 chr15: 94,341,751-94,345,046 MCTP2
    nsv3896620copy number variation1nstd102humanBenign GRCh37 chr15: 94,886,433-94,888,403 , GRCh38.p12 chr15: 94,343,204-94,345,174 MCTP2
    nsv6637754copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,942,904-95,041,259 , GRCh38.p12 chr15: 94,399,675-94,498,030 MCTP2
    nsv6291792copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,991,253-95,073,638 , GRCh38.p12 chr15: 94,448,024-94,530,409 MCTP2
    nsv7098941copy number variation1nstd102humanUncertain significance GRCh38 chr15: 94,302,663-94,352,488 , GRCh37.p13 chr15: 94,845,892-94,895,717 MCTP2
    nsv4675484copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,884,502-94,913,528 , GRCh38.p12 chr15: 94,341,273-94,370,299 MCTP2
    nsv4455562copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,848,894-94,866,975 , GRCh38.p12 chr15: 94,305,665-94,323,746 MCTP2
    nsv3898527copy number variation1nstd102humanBenign GRCh37 chr15: 94,781,904-94,828,466 , GRCh38.p12 chr15: 94,238,675-94,285,237 MCTP2, RPL26P5
    nsv4729253copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,814,176-94,861,302 , GRCh38.p12 chr15: 94,270,947-94,318,073 MCTP2, RPL26P5
    nsv3907358copy number variation1nstd102humanUncertain significance GRCh37 chr15: 94,818,923-95,388,951 , GRCh38.p12 chr15: 94,275,694-94,845,722 MCTP2, LOC105370986, 2 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 MCTP2, H3P40, 1616 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 MCTP2, RNU6-18P, 1442 more genes
    nsv4729092copy number variation1nstd102humanPathogenic GRCh37 chr15: 86,962,053-102,531,392 , GRCh38.p12 chr15: 86,418,822-101,981,189 MCTP2, CHD2, 272 more genes
    nsv4675149copy number variation1nstd102humanPathogenic GRCh37 chr15: 87,189,245-102,429,112 , GRCh38.p12 chr15: 86,646,014-101,888,909 MCTP2, TTLL13, 264 more genes
    nsv3908429copy number variation1nstd102humanPathogenic GRCh37 chr15: 90,346,994-102,354,798 , GRCh38.p12 chr15: 89,803,763-101,814,595 MCTP2, RPL31P55, 201 more genes
    nsv3899918copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,197,136-102,354,857 , GRCh38.p12 chr15: 91,653,906-101,814,654 MCTP2, SNRPCP18, 148 more genes
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 MCTP2, LOC105371009, 149 more genes
    nsv3919064copy number variation1nstd102humanPathogenic NCBI36 chr15: 91,542,950-100,200,996 , GRCh38 chr15: 93,198,717-101,843,270 , GRCh37 chr15: 93,741,946-102,383,473 MCTP2, LOC105371032, 126 more genes
    nsv3918825copy number variation1nstd102humanPathogenic GRCh37 chr15: 94,348,261-101,867,081 , GRCh38 chr15: 93,805,032-101,326,876 , NCBI36 chr15: 92,149,265-99,684,604 MCTP2, LOC440311, 107 more genes
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