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Items: 1 to 20 of 945

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144839insertion1nstd232human GRCh37.p13 chr17: 80,759,991-80,759,991 , GRCh38.p12 chr17: 82,802,115-82,802,115 TBCD
    nsv7141994insertion1nstd232human GRCh37.p13 chr17: 80,807,109-80,807,109 , GRCh38.p12 chr17: 82,849,233-82,849,233 TBCD
    nsv7140451insertion1nstd232human GRCh37.p13 chr17: 80,804,097-80,804,097 , GRCh38.p12 chr17: 82,846,221-82,846,221 TBCD
    nsv7137226insertion1nstd232human GRCh37.p13 chr17: 80,896,722-80,896,722 , GRCh38.p12 chr17: 82,938,846-82,938,846 , GRCh38.p12 chr17|NT_187612.1: 162,787-162,787 TBCD
    nsv7137148copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,656,331-81,009,672 , GRCh38.p12 chr17: 82,698,455-83,051,796 ZNF750, FN3KRP, 5 more genes
    nsv7098933copy number variation1nstd102humanUncertain significance GRCh38 chr17: 82,004,063-83,087,346 , GRCh37.p13 chr17: 79,961,939-81,045,222 ZNF750, LINC01970, 37 more genes
    nsv7098715copy number variation1nstd102humanPathogenic GRCh37 chr17: 79,539,041-81,052,322 , GRCh38.p12 chr17: 81,572,015-83,094,577 LOC105371939, LINC01970, 65 more genes
    nsv7095427copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,828,080-80,901,020 , GRCh38.p12 chr17: 82,870,204-82,943,144 TBCD, B3GNTL1
    nsv7095426copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 80,755,613-80,772,830 , GRCh38.p12 chr17: 82,797,737-82,814,954 TBCD
    nsv7095425copy number variation1nstd102humanPathogenic GRCh37 chr17: 80,710,070-80,901,020 , GRCh38.p12 chr17: 82,752,194-82,943,144 B3GNTL1, TBCD, 1 more genes
    nsv7095424copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,332,201-80,758,892 , GRCh38.p12 chr17: 82,374,325-82,801,016 CYBC1, TRX-CAT1-8, 15 more genes
    nsv7095374copy number variation1nstd102humanPathogenic GRCh37 chr17: 80,851,403-80,851,528 , GRCh38.p12 chr17: 82,893,527-82,893,652 TBCD
    nsv7095373copy number variation1nstd102humanPathogenic GRCh37 chr17: 80,847,524-80,901,020 , GRCh38.p12 chr17: 82,889,648-82,943,144 TBCD, B3GNTL1
    nsv7095370copy number variation1nstd102humanUncertain significance GRCh37 chr17: 79,477,716-80,900,339 , GRCh38.p12 chr17: 81,510,690-82,942,463 MIR6787, TBCD, 67 more genes
    nsv7093087copy number variation1nstd102humanUncertain significance GRCh37 chr17: 80,772,795-80,772,884 , GRCh38 chr17: 82,814,919-82,815,008 TBCD
    nsv7077597inversion1nstd229human GRCh38 chr17: 82,870,208-82,870,285 , GRCh37.p13 chr17: 80,828,084-80,828,161 TBCD
    nsv7076894inversion1nstd229human GRCh38 chr17: 82,792,114-82,983,211 , GRCh37.p13 chr17: 80,749,990-80,941,087 B3GNTL1, TBCD, 1 more genes
    nsv7075984inversion1nstd229human GRCh38 chr17: 82,937,313-82,941,314 , GRCh37.p13 chr17: 80,895,189-80,899,190 TBCD, B3GNTL1
    nsv7074038inversion1nstd229human GRCh38 chr17: 82,941,202-82,947,101 , GRCh37.p13 chr17: 80,899,078-80,904,977 TBCD, B3GNTL1
    nsv7071250inversion1nstd229human GRCh38 chr17: 82,926,750-82,934,489 , GRCh37.p13 chr17: 80,884,626-80,892,365 TBCD
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