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Items: 1 to 20 of 118

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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
    nsv7147849copy number variation1nstd232human GRCh37.p13 chr17: 27,185,502-27,185,590 , GRCh38.p12 chr17: 28,858,484-28,858,572 ERAL1
    nsv7140507copy number variation1nstd232human GRCh37.p13 chr17: 27,186,128-27,186,216 , GRCh38.p12 chr17: 28,859,110-28,859,198 ERAL1
    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
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6997427copy number variation1nstd229human GRCh38 chr17: 28,857,256-28,859,444 , GRCh37.p13 chr17: 27,184,274-27,186,462 MIR451A, ERAL1, 1 more genes
    nsv6995506copy number variation1nstd229human GRCh38 chr17: 28,826,930-28,857,088 , GRCh37.p13 chr17: 27,153,948-27,184,106 ERAL1, FAM222B
    nsv6981917copy number variation1nstd229human GRCh38 chr17: 28,805,032-28,929,082 , GRCh37.p13 chr17: 27,132,050-27,256,100 MIR451A, FAM222B, 8 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
    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
    nsv6133228copy number variation1nstd213human GRCh37 chr17: 25,300,000-27,290,001 , GRCh38.p12 chr17: 26,972,974-28,962,983 LGALS9, RPL23A, 82 more genes
    nsv5945123copy number variation1nstd209human GRCh38 chr17: 28,847,070-28,853,039 , GRCh37.p13 chr17: 27,174,088-27,180,057 ERAL1, FAM222B
    nsv5527975copy number variation1nstd206human GRCh38 chr17: 28,847,073-28,853,052 , GRCh37.p13 chr17: 27,174,091-27,180,070 FAM222B, ERAL1
    nsv5527237copy number variation1nstd206human GRCh38 chr17: 28,844,562-28,871,621 , GRCh37.p13 chr17: 27,171,580-27,198,639 ERAL1, FAM222B, 4 more genes
    nsv5519760copy number variation1nstd206human GRCh38 chr17: 28,847,137-28,853,063 , GRCh37.p13 chr17: 27,174,155-27,180,081 ERAL1, FAM222B
    nsv5010271copy number variation1nstd200human GRCh38 chr17: 28,856,904-28,859,697 , GRCh37.p13 chr17: 27,183,922-27,186,715 MIR451A, MIR451B, 3 more genes
    nsv4864592copy number variation1nstd200human GRCh37 chr17: 27,174,024-27,180,122 , GRCh38.p12 chr17: 28,847,006-28,853,104 FAM222B, ERAL1
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
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