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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6834832copy number variation1nstd229human GRCh38 chr7: 87,334,651-87,337,660 , GRCh37.p13 chr7: 86,963,967-86,966,976 TP53TG1
    nsv6831632copy number variation1nstd229human GRCh38 chr7: 86,090,518-87,706,185 , GRCh37.p13 chr7: 85,719,834-87,335,501 ABCB1, TP53TG1, 12 more genes
    nsv6824731copy number variation1nstd229human GRCh38 chr7: 87,334,615-87,334,669 , GRCh37.p13 chr7: 86,963,931-86,963,985 TP53TG1
    nsv6822073copy number variation1nstd229human GRCh38 chr7: 86,140,900-87,353,128 , GRCh37.p13 chr7: 85,770,216-86,982,444 TMEM243, DMTF1, 8 more genes
    nsv6821698copy number variation1nstd229human GRCh38 chr7: 87,287,883-87,337,493 , GRCh37.p13 chr7: 86,917,199-86,966,809 TP53TG1
    nsv6819432copy number variation1nstd229human GRCh38 chr7: 87,253,014-87,326,796 , GRCh37.p13 chr7: 86,882,330-86,956,112 TP53TG1
    nsv6818739copy number variation1nstd229human GRCh38 chr7: 84,598,855-91,861,148 , GRCh37.p13 chr7: 84,228,171-91,490,462 CDK14, LOC101409256, 59 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
    nsv6632462copy number variation1nstd224human GRCh37 chr7: 86,944,642-87,517,349 , GRCh38.p12 chr7: 87,315,326-87,888,034 ABCB1, ABCB4, 6 more genes
    nsv6615246copy number variation1nstd223human GRCh38 chr7: 87,253,014-87,326,798 , GRCh37.p13 chr7: 86,882,330-86,956,114 TP53TG1
    nsv6612386copy number variation1nstd223human GRCh38 chr7: 87,287,883-87,337,489 , GRCh37.p13 chr7: 86,917,199-86,966,805 TP53TG1
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313801copy number variation1nstd102humanPathogenic GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825 SOCS5P1, FAM133B, 140 more genes
    nsv6245541mobile element insertion1nstd215human GRCh38 chr7: 87,339,203-87,339,203 , GRCh37.p13 chr7: 86,968,519-86,968,519 TP53TG1
    nsv6136273copy number variation1nstd213human GRCh37 chr7: 86,700,000-87,470,001 , GRCh38.p12 chr7: 87,070,684-87,840,686 ABCB1, CROT, 9 more genes
    nsv6136262copy number variation1nstd213human GRCh37 chr7: 77,010,000-90,950,001 , GRCh38.p12 chr7: 77,380,683-91,320,686 , GRM3, 118 more genes
    nsv6135785copy number variation1nstd213human GRCh37 chr7: 76,690,000-99,250,001 , GRCh38.p12 chr7: 77,060,683-99,652,378 , ASNS, 283 more genes
    nsv6011879copy number variation1nstd212human GRCh38 chr7: 87,345,722-87,346,387 , GRCh37.p13 chr7: 86,975,038-86,975,703 CROT, TP53TG1
    nsv5977915inversion1nstd209human GRCh38 chr7: 86,525,777-88,855,329 , GRCh37.p13 chr7: 86,155,093-88,484,643 , GRM3, 31 more genes
    nsv5917072copy number variation1nstd209human GRCh38 chr7: 87,338,527-87,338,848 , GRCh37.p13 chr7: 86,967,843-86,968,164 TP53TG1
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