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Items: 1 to 20 of 342

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5966013insertion1nstd209human GRCh38 chr9: 131,130,150-131,130,150 , GRCh37.p13 chr9: 134,005,537-134,005,537 NUP214
    nsv5965814insertion1nstd209human GRCh38 chr9: 131,193,629-131,193,629 , GRCh37.p13 chr9: 134,069,016-134,069,016 NUP214
    nsv5962049insertion1nstd209human GRCh38 chr9: 131,206,148-131,206,148 , GRCh37.p13 chr9: 134,081,535-134,081,535 NUP214
    nsv5728891mobile element insertion1nstd211human GRCh38 chr9: 131,124,031-131,124,031 , GRCh37.p13 chr9: 133,999,418-133,999,418 NUP214
    nsv5716753mobile element insertion1nstd211human GRCh38 chr9: 131,131,652-131,131,652 , GRCh37.p13 chr9: 134,007,039-134,007,039 NUP214
    nsv5715742mobile element insertion1nstd211human GRCh38 chr9: 131,126,565-131,126,565 , GRCh37.p13 chr9: 134,001,952-134,001,952 RNU6-881P, NUP214
    nsv5712578mobile element insertion1nstd211human GRCh38 chr9: 131,192,195-131,192,195 , GRCh37.p13 chr9: 134,067,582-134,067,582 NUP214
    nsv5490867copy number variation1nstd206human GRCh38 chr9: 131,154,477-131,156,233 , GRCh37.p13 chr9: 134,029,864-134,031,620 NUP214
    nsv5476073copy number variation1nstd206human GRCh38 chr9: 131,204,448-131,204,498 , GRCh37.p13 chr9: 134,079,835-134,079,885 NUP214
    nsv5475965copy number variation1nstd206human GRCh38 chr9: 131,215,919-131,216,229 , GRCh37.p13 chr9: 134,091,306-134,091,616 NUP214
    nsv5474291copy number variation1nstd206human GRCh38 chr9: 131,193,876-131,194,876 , GRCh37.p13 chr9: 134,069,263-134,070,263 NUP214
    nsv5379536translocation1nstd200human GRCh38 chr9: 131,230,792-131,230,792 , GRCh38 chr9: 131,423,585-131,423,585 , GRCh37.p13 chr9: 134,106,179-134,106,179 , GRCh37.p13 chr9: 134,298,972-134,298,972 NUP214
    nsv5379535translocation1nstd200human GRCh38 chr9: 131,162,050-131,162,050 , GRCh38 chr9: 131,161,680-131,161,680 , GRCh37.p13 chr9: 134,037,067-134,037,067 , GRCh37.p13 chr9: 134,037,437-134,037,437 NUP214
    nsv5379534translocation1nstd200human GRCh38 chr9: 131,161,936-131,161,936 , GRCh38 chr9: 131,160,831-131,160,831 , GRCh37.p13 chr9: 134,036,218-134,036,218 , GRCh37.p13 chr9: 134,037,323-134,037,323 NUP214
    nsv5373148translocation1nstd200human GRCh38 chr9: 131,221,528-131,221,528 , GRCh38 chr9: 131,221,593-131,221,593 , GRCh37.p13 chr9: 134,096,980-134,096,980 , GRCh37.p13 chr9: 134,096,915-134,096,915 NUP214
    nsv5354143translocation1nstd200human GRCh38 chr9: 131,131,642-131,131,642 , GRCh38 chr22: 40,502,838-40,502,838 , GRCh37.p13 chr9: 134,007,029-134,007,029 , GRCh37.p13 chr22: 40,898,842-40,898,842 NUP214, MRTFA
    nsv5335807translocation1nstd200human GRCh37 chr9: 134,037,437-134,037,437 , GRCh37 chr9: 134,037,067-134,037,067 , GRCh38.p12 chr9: 131,162,050-131,162,050 , GRCh38.p12 chr9: 131,161,680-131,161,680 NUP214
    nsv5334493translocation1nstd200human GRCh37 chr9: 134,036,218-134,036,218 , GRCh37 chr9: 134,037,323-134,037,323 , GRCh38.p12 chr9: 131,161,936-131,161,936 , GRCh38.p12 chr9: 131,160,831-131,160,831 NUP214
    nsv5314598copy number variation1nstd204human GRCh38.p13 chr9: 131,154,513-131,156,203 , GRCh37.p13 chr9: 134,029,900-134,031,590 NUP214
    nsv5259486copy number variation1nstd204human GRCh38.p13 chr9: 131,128,039-131,130,338 , GRCh37.p13 chr9: 134,003,426-134,005,725 NUP214
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