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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148088copy number variation1nstd102humanUncertain significance GRCh37 chr17: 25,263,507-27,829,791 , GRCh38.p12 chr17: 26,936,481-29,502,773 RNU4-34P, RNU6-711P, 95 more genes
    nsv7095084copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155 RNU6-1267P, PIPOX, 114 more genes
    nsv7094962copy number variation1nstd102humanUncertain significance GRCh37 chr17: 26,684,694-27,581,367 , GRCh38.p12 chr17: 28,357,671-29,254,349 FLOT2, SPAG5-AS1, 50 more genes
    nsv7067872inversion1nstd229human GRCh38 chr17: 28,416,471-28,817,211 , GRCh37.p13 chr17: 26,840,020-27,144,229 SUPT6H, SPAG5-AS1, 25 more genes
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6989413copy number variation1nstd229human GRCh38 chr17: 28,628,269-28,696,734 , GRCh37.p13 chr17: 26,955,287-27,023,752 SUPT6H, RPS12P28, 2 more genes
    nsv6983677copy number variation1nstd229human GRCh38 chr17: 28,389,847-28,690,853 , GRCh37.p13 chr17: 26,840,020-27,017,871 LOC101060112, SPAG5, 15 more genes
    nsv6981563copy number variation1nstd229human GRCh38 chr17: 28,642,432-28,647,317 , GRCh37.p13 chr17: 26,969,450-26,974,335 BLTP2, SDF2
    nsv6585001inversion1nstd223human GRCh38 chr17: 28,649,335-28,650,091 , GRCh37.p13 chr17: 26,976,353-26,977,109 SDF2
    nsv6515002copy number variation1nstd223human GRCh38 chr17: 28,371,101-28,759,756 , GRCh37.p13 chr17: 26,840,020-27,086,774 FAM222B, SDF2, 26 more genes
    nsv6505570copy number variation1nstd223human GRCh38 chr17: 28,646,174-28,646,455 , GRCh37.p13 chr17: 26,973,192-26,973,473 SDF2
    nsv6502917copy number variation1nstd223human GRCh38 chr17: 28,650,846-28,651,101 , GRCh37.p13 chr17: 26,977,864-26,978,119 SDF2
    nsv6501768copy number variation1nstd223human GRCh38 chr17: 28,649,636-28,650,616 , GRCh37.p13 chr17: 26,976,654-26,977,634 SDF2
    nsv6496974copy number variation1nstd223human GRCh38 chr17: 28,654,864-28,664,328 , GRCh37.p13 chr17: 26,981,882-26,991,346 SUPT6H, SDF2, 1 more genes
    nsv6314042copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214 TAOK1, TNFAIP1, 131 more genes
    nsv6250721mobile element insertion1nstd215human GRCh38 chr17: 28,650,844-28,650,844 , GRCh37.p13 chr17: 26,977,862-26,977,862 SDF2
    nsv6145513copy number variation1nstd206human GRCh38 chr17: 28,654,728-28,664,398 , GRCh37.p13 chr17: 26,981,746-26,991,416 SDF2, RPS12P28, 1 more genes
    nsv6133349copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,060,001 , GRCh38.p12 chr17: 28,642,982-28,732,983 RPL23A, SDF2, 11 more genes
    nsv6133232copy number variation1nstd213human GRCh37 chr17: 26,970,000-27,750,001 , GRCh38.p12 chr17: 28,642,982-29,422,983 CRYBA1, FLOT2, 37 more genes
    nsv6133229copy number variation1nstd213human GRCh37 chr17: 25,300,000-32,120,001 , GRCh38.p12 chr17: 26,972,974-33,792,982 BLMH, CPD, 197 more genes
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