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Items: 1 to 20 of 104

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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
    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
    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
    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
    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
    nsv5149859mobile element insertion1nstd203human GRCh38 chr17: 28,720,560-28,720,571 , GRCh37.p13 chr17: 27,047,578-27,047,589 SNORD42B, RPL23A
    nsv5023902copy number variation1nstd200human GRCh38 chr17: 28,371,101-28,759,758 , GRCh37.p13 chr17: 26,840,020-27,086,776 RSKR, TRAF4, 26 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675321copy number variation1nstd102humanPathogenic GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689 ABHD15, LOC100420408, 112 more genes
    nsv4512823mobile element insertion1nstd166human GRCh37.p13 chr17: 27,047,578-27,047,578 , GRCh38.p12 chr17: 28,720,560-28,720,560 SNORD42B, RPL23A
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4379025copy number variation1nstd173human GRCh37 chr17: 25,307,567-27,710,963 , GRCh38.p12 chr17: 26,980,541-29,383,945 , MIR451A, 91 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4247886copy number variation1nstd166human GRCh37.p13 chr17: 27,049,319-27,049,438 , GRCh38.p12 chr17: 28,722,301-28,722,420 RPL23A, SNORD4B, 3 more genes
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