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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095086copy number variation1nstd102humanPathogenic GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139 LOC107984990, ADAP2, 59 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
    nsv7062182inversion1nstd229human GRCh38 chr17: 27,487,612-31,414,648 , GRCh37.p13 chr17: 25,814,638-29,741,666 ERAL1, SARM1, 140 more genes
    nsv7059192inversion1nstd229human GRCh38 chr17: 30,069,297-30,546,697 , GRCh37.p13 chr17: 28,396,315-28,873,715 SLC6A4, LOC105371720, 13 more genes
    nsv7058412inversion1nstd229human GRCh38 chr17: 30,021,943-32,643,975 , GRCh37.p13 chr17: 28,348,961-30,970,993 RNU6-990P, LOC105371730, 81 more genes
    nsv6982880copy number variation1nstd229human GRCh38 chr17: 30,114,601-30,117,000 , GRCh37.p13 chr17: 28,441,619-28,444,018 MIR3184, MIR423, 1 more genes
    nsv6980451copy number variation1nstd229human GRCh38 chr17: 29,103,792-32,176,512 , GRCh37.p13 chr17: 27,430,810-30,503,531 SMURF2P1-LRRC37BP1, RNU6-990P, 90 more genes
    nsv6978581copy number variation1nstd229human GRCh38 chr17: 30,041,301-30,206,800 , GRCh37.p13 chr17: 28,368,319-28,533,818 SLC6A4, EFCAB5, 5 more genes
    nsv6512579copy number variation1nstd223human GRCh38 chr17: 30,114,302-30,115,741 , GRCh37.p13 chr17: 28,441,320-28,442,759 MIR423, NSRP1, 1 more genes
    nsv6133298copy number variation1nstd213human GRCh37 chr17: 27,880,000-28,800,001 , GRCh38.p12 chr17: 29,552,982-30,472,983 BLMH, CPD, 23 more genes
    nsv6133235copy number variation1nstd213human GRCh37 chr17: 28,370,000-29,090,001 , GRCh38.p12 chr17: 30,042,982-30,762,983 ALOX12P1, TBC1D29P, 26 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
    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
    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
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4370646copy number variation1nstd173human GRCh37 chr17: 27,870,962-28,495,223 , GRCh38.p12 chr17: 29,543,944-30,168,205 RNU6-920P, ABHD15, 16 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
    nsv3972367copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446 ASIC2, AK4P1, 190 more genes
    nsv3919950copy number variation1nstd102humanPathogenic NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020 MIR365B, EFCAB5, 105 more genes
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