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Items: 1 to 20 of 394

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5926622copy number variation1nstd209human GRCh38 chr8: 47,906,391-47,907,361 , GRCh37.p13 chr8: 48,818,951-48,819,921 PRKDC
    nsv5910931copy number variation1nstd209human GRCh38 chr8: 47,886,421-47,886,718 , GRCh37.p13 chr8: 48,798,982-48,799,279 PRKDC
    nsv5714450mobile element insertion1nstd211human GRCh38 chr8: 47,868,433-47,868,433 , GRCh37.p13 chr8: 48,780,994-48,780,994 PRKDC
    nsv5632730insertion1nstd207human GRCh38 chr8: 47,863,624-47,863,624 , GRCh37.p13 chr8: 48,776,185-48,776,185 PRKDC
    nsv5630478insertion1nstd207human GRCh38 chr8: 47,952,806-47,952,806 , GRCh37.p13 chr8: 48,865,366-48,865,366 PRKDC
    nsv5628663insertion1nstd207human GRCh38 chr8: 47,871,747-47,871,747 , GRCh37.p13 chr8: 48,784,308-48,784,308 PRKDC
    nsv5564477copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,701,819 , GRCh38.p12 chr8: 47,774,153-47,789,258 PRKDC
    nsv5492875copy number variation1nstd206human GRCh38 chr8: 47,831,492-47,831,574 , GRCh37.p13 chr8: 48,744,053-48,744,135 PRKDC
    nsv5489649copy number variation1nstd206human GRCh38 chr8: 47,841,117-47,846,119 , GRCh37.p13 chr8: 48,753,678-48,758,680 PRKDC
    nsv5488900copy number variation1nstd206human GRCh38 chr8: 47,794,970-47,795,271 , GRCh37.p13 chr8: 48,707,531-48,707,832 PRKDC
    nsv5482117copy number variation1nstd206human GRCh38 chr8: 47,871,747-47,871,889 , GRCh37.p13 chr8: 48,784,308-48,784,450 PRKDC
    nsv5481798copy number variation1nstd206human GRCh38 chr8: 47,833,762-47,833,881 , GRCh37.p13 chr8: 48,746,323-48,746,442 PRKDC
    nsv5481651copy number variation1nstd206human GRCh38 chr8: 47,779,580-47,779,945 , GRCh37.p13 chr8: 48,692,141-48,692,506 PRKDC
    nsv5477452copy number variation1nstd206human GRCh38 chr8: 47,796,726-47,796,844 , GRCh37.p13 chr8: 48,709,287-48,709,405 PRKDC
    nsv5477401copy number variation1nstd206human GRCh38 chr8: 47,906,391-47,907,368 , GRCh37.p13 chr8: 48,818,951-48,819,928 PRKDC
    nsv5475255copy number variation1nstd206human GRCh38 chr8: 47,957,763-47,959,017 , GRCh37.p13 chr8: 48,870,323-48,871,577 MCM4, PRKDC
    nsv5381645copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,839,734-48,872,706 , GRCh38.p12 chr8: 47,927,174-47,960,146 LOC105375818, MCM4, 1 more genes
    nsv5381478copy number variation1nstd102humanUncertain significance GRCh37 chr8: 48,686,714-48,713,567 , GRCh38.p12 chr8: 47,774,153-47,801,006 PRKDC
    nsv5371631translocation1nstd200human GRCh38 chr8: 47,833,881-47,833,881 , GRCh38 chr8: 47,833,762-47,833,762 , GRCh37.p13 chr8: 48,746,323-48,746,323 , GRCh37.p13 chr8: 48,746,442-48,746,442 PRKDC
    nsv5371630translocation1nstd200human GRCh38 chr8: 47,774,412-47,774,412 , GRCh38 chr8: 47,774,573-47,774,573 , GRCh37.p13 chr8: 48,686,973-48,686,973 , GRCh37.p13 chr8: 48,687,134-48,687,134 PRKDC
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