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Items: 1 to 20 of 565

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097368copy number variation1nstd102humanUncertain significance GRCh37 chr7: 33,217,070-34,888,295 , GRCh38.p12 chr7: 33,177,458-34,848,683 RN7SL132P, NPSR1, 9 more genes
    nsv7054607inversion1nstd229human GRCh38 chr7: 34,137,694-34,142,184 , GRCh37.p13 chr7: 34,177,306-34,181,796 BMPER
    nsv6837707copy number variation1nstd229human GRCh38 chr7: 34,124,910-34,125,081 , GRCh37.p13 chr7: 34,164,522-34,164,693 BMPER
    nsv6836638copy number variation1nstd229human GRCh38 chr7: 34,077,433-34,083,813 , GRCh37.p13 chr7: 34,117,045-34,123,425 BMPER
    nsv6832572copy number variation1nstd229human GRCh38 chr7: 33,910,746-33,910,769 , GRCh37.p13 chr7: 33,950,358-33,950,381 BMPER
    nsv6832077copy number variation1nstd229human GRCh38 chr7: 33,961,723-34,013,229 , GRCh37.p13 chr7: 34,001,335-34,052,841 BMPER
    nsv6831749copy number variation1nstd229human GRCh38 chr7: 33,955,801-33,960,100 , GRCh37.p13 chr7: 33,995,413-33,999,712 BMPER
    nsv6830184copy number variation1nstd229human GRCh38 chr7: 34,014,203-34,017,998 , GRCh37.p13 chr7: 34,053,815-34,057,610 BMPER
    nsv6828714copy number variation1nstd229human GRCh38 chr7: 34,083,580-34,084,520 , GRCh37.p13 chr7: 34,123,192-34,124,132 BMPER
    nsv6828145copy number variation1nstd229human GRCh38 chr7: 34,099,030-34,099,073 , GRCh37.p13 chr7: 34,138,642-34,138,685 BMPER
    nsv6827525copy number variation1nstd229human GRCh38 chr7: 33,939,257-33,945,254 , GRCh37.p13 chr7: 33,978,869-33,984,866 BMPER
    nsv6826389copy number variation1nstd229human GRCh38 chr7: 34,090,797-34,095,408 , GRCh37.p13 chr7: 34,130,409-34,135,020 BMPER
    nsv6825951copy number variation1nstd229human GRCh38 chr7: 34,155,843-34,156,034 , GRCh37.p13 chr7: 34,195,455-34,195,646 BMPER
    nsv6824938copy number variation1nstd229human GRCh38 chr7: 34,024,398-34,028,894 , GRCh37.p13 chr7: 34,064,010-34,068,506 BMPER
    nsv6824863copy number variation1nstd229human GRCh38 chr7: 34,050,318-34,075,203 , GRCh37.p13 chr7: 34,089,930-34,114,815 BMPER
    nsv6824166copy number variation1nstd229human GRCh38 chr7: 34,097,336-35,381,641 , GRCh37.p13 chr7: 34,136,948-35,421,251 LOC401324, NPSR1, 13 more genes
    nsv6822609copy number variation1nstd229human GRCh38 chr7: 34,024,792-34,031,934 , GRCh37.p13 chr7: 34,064,404-34,071,546 BMPER
    nsv6821861copy number variation1nstd229human GRCh38 chr7: 33,922,894-33,925,541 , GRCh37.p13 chr7: 33,962,506-33,965,153 BMPER
    nsv6821615copy number variation1nstd229human GRCh38 chr7: 33,730,739-34,432,306 , GRCh37.p13 chr7: 33,770,351-34,471,918 BMPER, RNU6-438P, 1 more genes
    nsv6820359copy number variation1nstd229human GRCh38 chr7: 33,966,554-34,711,618 , GRCh37.p13 chr7: 34,006,166-34,751,230 BMPER, NPSR1, 3 more genes
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