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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053084inversion1nstd229human GRCh38 chr6: 22,043,616-23,034,796 , GRCh37.p13 chr6: 22,043,845-23,035,025 LOC102724736, LINC03005, 7 more genes
    nsv7051368inversion1nstd229human GRCh38 chr6: 20,052,222-24,804,874 , GRCh37.p13 chr6: 20,052,453-24,805,102 LOC102724736, LOC105374966, 51 more genes
    nsv7039826inversion1nstd229human GRCh38 chr6: 19,226,276-22,428,371 , GRCh37.p13 chr6: 19,226,507-22,428,600 RN7SKP240, LOC107986578, 32 more genes
    nsv6796076copy number variation1nstd229human GRCh38 chr6: 22,135,608-22,138,380 , GRCh37.p13 chr6: 22,135,837-22,138,609 CASC15, NBAT1
    nsv6784769copy number variation1nstd229human GRCh38 chr6: 22,144,345-22,151,875 , GRCh37.p13 chr6: 22,144,574-22,152,104 CASC15, NBAT1
    nsv6636333copy number variation1nstd102humanPathogenic GRCh37 chr6: 12,005,630-22,849,647 , GRCh38.p12 chr6: 12,005,397-22,849,418 SOX4, MDH1P2, 136 more genes
    nsv6568372inversion1nstd223human GRCh38 chr6: 21,391,567-22,908,554 , GRCh37.p13 chr6: 21,391,798-22,908,783 LOC105374971, RN7SKP240, 12 more genes
    nsv6563104inversion1nstd223human GRCh38 chr6: 20,052,171-24,804,275 , GRCh37.p13 chr6: 20,052,402-24,804,503 HDGFL1, LOC105374976, 51 more genes
    nsv6412639copy number variation1nstd223human GRCh38 chr6: 22,120,201-22,198,400 , GRCh37.p13 chr6: 22,120,430-22,198,629 CASC15, NBAT1
    nsv6135837copy number variation1nstd213human GRCh37 chr6: 22,040,000-22,270,001 , GRCh38.p12 chr6: 22,039,771-22,269,772 CASC15, NBAT1, 1 more genes
    nsv5961744insertion1nstd209human GRCh38 chr6: 22,141,994-22,141,994 , GRCh37.p13 chr6: 22,142,223-22,142,223 NBAT1, CASC15
    nsv5714595mobile element insertion1nstd211human GRCh38 chr6: 22,132,632-22,132,632 , GRCh37.p13 chr6: 22,132,861-22,132,861 CASC15, NBAT1
    nsv5090059mobile element insertion1nstd203human GRCh38 chr6: 22,145,866-22,145,882 , GRCh37.p13 chr6: 22,146,095-22,146,111 CASC15, NBAT1
    nsv5030523inversion1nstd200human GRCh38 chr6: 21,391,567-22,908,554 , GRCh37.p13 chr6: 21,391,798-22,908,783 LINC00581, HDGFL1, 12 more genes
    nsv4934508copy number variation1nstd200human GRCh38 chr6: 22,144,342-22,151,878 , GRCh37.p13 chr6: 22,144,571-22,152,107 CASC15, NBAT1
    nsv4933135copy number variation1nstd200human GRCh38 chr6: 22,135,608-22,138,377 , GRCh37.p13 chr6: 22,135,837-22,138,606 NBAT1, CASC15
    nsv4828543copy number variation1nstd200human GRCh37 chr6: 22,144,571-22,152,107 , GRCh38.p12 chr6: 22,144,342-22,151,878 CASC15, NBAT1
    nsv4815574copy number variation1nstd200human GRCh37 chr6: 22,135,837-22,138,606 , GRCh38.p12 chr6: 22,135,608-22,138,377 NBAT1, CASC15
    nsv4482881mobile element insertion1nstd166human GRCh37.p13 chr6: 22,141,727-22,141,727 , GRCh38.p12 chr6: 22,141,498-22,141,498 CASC15, NBAT1
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
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