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Items: 1 to 20 of 105

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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
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv6991825copy number variation1nstd229human GRCh38 chr17: 28,337,489-28,337,845 , GRCh37.p13 chr17: 26,664,515-26,664,871 , GRCh37.p13 chr17|NW_003871090.1: 19,357-19,713 TNFAIP1
    nsv6984076copy number variation1nstd229human GRCh38 chr17: 28,344,625-28,421,897 , GRCh37.p13 chr17|NW_003871090.1: 26,493-103,758 , GRCh37.p13 chr17: 26,671,651-26,748,915 VTN, H3P41, 7 more genes
    nsv6979708copy number variation1nstd229human GRCh38 chr17: 28,342,201-28,348,200 , GRCh37.p13 chr17|NW_003871090.1: 24,069-30,068 , GRCh37.p13 chr17: 26,669,227-26,675,226 TNFAIP1, POLDIP2
    nsv6508138copy number variation1nstd223human GRCh38 chr17: 28,308,852-28,403,730 , GRCh37.p13 chr17: 26,645,159-26,730,748 , GRCh37.p13 chr17|NW_003871090.1: 1-85,591 TNFAIP1, POLDIP2, 8 more genes
    nsv6498261copy number variation1nstd223human GRCh38 chr17: 28,346,501-28,430,000 , GRCh37.p13 chr17|NW_003871090.1: 28,369-111,861 , GRCh37.p13 chr17: 26,673,527-26,757,018 POLDIP2, TMEM199, 7 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
    nsv6133231copy number variation1nstd213human GRCh37 chr17: 25,820,000-26,720,001 , GRCh38.p12 chr17: 27,492,974-28,392,982 LGALS9, NOS2, 30 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
    nsv5705213mobile element insertion1nstd211human GRCh38 chr17: 28,346,390-28,346,390 , GRCh37.p13 chr17|NW_003871090.1: 28,258-28,258 , GRCh37.p13 chr17: 26,673,416-26,673,416 TNFAIP1, POLDIP2
    nsv5429842mobile element insertion1nstd206human GRCh38 chr17: 28,346,390-28,346,441 , GRCh37.p13 chr17|NW_003871090.1: 28,258-28,309 , GRCh37.p13 chr17: 26,673,416-26,673,467 POLDIP2, TNFAIP1
    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
    nsv4531981copy number variation1nstd166human GRCh37.p13 chr17: 26,673,825-26,757,026 , GRCh38.p12 chr17: 28,346,799-28,430,008 TNFAIP1, VTN, 7 more genes
    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
    nsv4243070copy number variation1nstd166human GRCh37.p13 chr17: 26,517,014-26,775,312 , GRCh38.p12 chr17: 28,189,988-28,448,294 IFT20, H3P41, 17 more genes
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