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Items: 1 to 20 of 130

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7053235inversion1nstd229human GRCh38 chr7: 17,455,146-18,223,221 , GRCh37.p13 chr7: 17,494,770-18,262,844 SNX13, PRPS1L1, 6 more genes
    nsv7053118inversion1nstd229human GRCh38 chr7: 17,057,438-20,155,989 , GRCh37.p13 chr7: 17,097,062-20,195,612 MIR1302-6, LOC100419901, 29 more genes
    nsv6817335copy number variation1nstd229human GRCh38 chr7: 18,067,161-19,210,067 , GRCh37.p13 chr7: 18,106,784-19,249,690 HDAC9, HDAC9-AS1, 6 more genes
    nsv6808366copy number variation1nstd229human GRCh38 chr7: 17,821,383-18,325,020 , GRCh37.p13 chr7: 17,861,006-18,364,643 MIR1302-6, PRPS1L1, 3 more genes
    nsv6801914copy number variation1nstd229human GRCh38 chr7: 17,935,837-18,198,742 , GRCh37.p13 chr7: 17,975,460-18,238,365 SNX13, HDAC9, 3 more genes
    nsv6634397copy number variation1nstd102humanPathogenic GRCh37 chr7: 43,360-19,485,604 , GRCh38.p12 chr7: 43,360-19,445,981 DNAAF5, FSCN1, 277 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632061copy number variation1nstd224human GRCh37 chr7: 17,865,659-18,504,411 , GRCh38.p12 chr7: 17,826,036-18,464,788 SNX13, MIR1302-6, 3 more genes
    nsv6609063copy number variation1nstd223human GRCh38 chr7: 17,821,383-18,325,020 , GRCh37.p13 chr7: 17,861,006-18,364,643 MIR1302-6, PRPS1L1, 3 more genes
    nsv6608233copy number variation1nstd223human GRCh38 chr7: 18,121,700-18,140,975 , GRCh37.p13 chr7: 18,161,323-18,180,598 HDAC9, MIR1302-6
    nsv6603657copy number variation1nstd223human GRCh38 chr7: 17,935,837-18,198,742 , GRCh37.p13 chr7: 17,975,460-18,238,365 PRPS1L1, MIR1302-6, 3 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313854copy number variation1nstd102humanPathogenic GRCh37 chr7: 9,358,316-20,982,082 , GRCh38.p12 chr7: 9,318,686-20,942,463 LOC107986766, RPL36AP26, 115 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6136983copy number variation1nstd213human GRCh37 chr7: 17,860,000-20,080,001 , GRCh38.p12 chr7: 17,820,377-20,040,378 TWIST1, SNX13, 19 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv4953446copy number variation1nstd200human GRCh38 chr7: 17,821,383-18,325,023 , GRCh37.p13 chr7: 17,861,006-18,364,646 , SNX13, 4 more genes
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4768371copy number variation1nstd102humanPathogenic GRCh37 chr7: 14,470,668-20,385,165 , GRCh38.p12 chr7: 14,431,043-20,345,542 HDAC9, LOC101927668, 60 more genes
    nsv4729607copy number variation1nstd102humanLikely benign GRCh37 chr7: 17,865,965-18,361,645 , GRCh38.p12 chr7: 17,826,342-18,322,022 SNX13, MRM3P2, 3 more genes
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