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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6993746copy number variation1nstd229human GRCh38 chr17: 35,136,760-35,142,986 , GRCh37.p13 chr17: 33,463,779-33,470,005 NLE1
    nsv6993100copy number variation1nstd229human GRCh38 chr17: 35,132,705-35,132,805 , GRCh37.p13 chr17: 33,459,724-33,459,824 NLE1
    nsv6989047copy number variation1nstd229human GRCh38 chr17: 35,123,112-35,128,030 , GRCh37.p13 chr17: 33,450,131-33,455,049 NLE1, FNDC8
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6585402inversion1nstd223human GRCh38 chr17: 35,142,644-35,143,002 , GRCh37.p13 chr17: 33,469,663-33,470,021 NLE1
    nsv6499851copy number variation1nstd223human GRCh38 chr17: 34,998,758-35,727,531 , GRCh37.p13 chr17: 33,325,777-34,034,851 FNDC8, LOC101060119, 32 more genes
    nsv6497653copy number variation1nstd223human GRCh38 chr17: 35,123,112-35,128,026 , GRCh37.p13 chr17: 33,450,131-33,455,045 NLE1, FNDC8
    nsv6497486copy number variation1nstd223human GRCh38 chr17: 34,547,647-35,364,191 , GRCh37.p13 chr17: 32,874,666-33,691,210 LOC105371742, ZNF830, 19 more genes
    nsv6250755mobile element insertion1nstd215human GRCh38 chr17: 35,133,666-35,133,666 , GRCh37.p13 chr17: 33,460,685-33,460,685 NLE1
    nsv6133353copy number variation1nstd213human GRCh37 chr17: 33,210,000-34,670,001 , GRCh38.p12 chr17: 34,882,981-35,919,248 AP2B1, E2F3P1, 48 more genes
    nsv6133243copy number variation1nstd213human GRCh37 chr17: 33,420,000-33,600,001 , GRCh38.p12 chr17: 35,092,981-35,272,982 RAD51D, NLE1, 7 more genes
    nsv6133050copy number variation1nstd213human GRCh37 chr17: 32,790,000-34,510,001 , GRCh38.p12 chr17: 34,462,981-35,919,248 AP2B1, E2F3P1, 53 more genes
    nsv6114617mobile element insertion1nstd186human GRCh37 chr17: 33,460,685-33,460,736 , GRCh38.p12 chr17: 35,133,666-35,133,717 NLE1
    nsv6093214insertion1nstd212human GRCh38 chr17: 35,133,662-35,133,662 , GRCh37.p13 chr17: 33,460,681-33,460,681 NLE1
    nsv5975834insertion1nstd209human GRCh38 chr17: 35,133,653-35,133,653 , GRCh37.p13 chr17: 33,460,672-33,460,672 NLE1
    nsv5935205copy number variation1nstd209human GRCh38 chr17: 35,132,909-35,133,001 , GRCh37.p13 chr17: 33,459,928-33,460,020 NLE1
    nsv5698992mobile element insertion2nstd211human GRCh38 chr17: 35,133,666-35,133,666 , GRCh37.p13 chr17: 33,460,685-33,460,685 NLE1
    nsv5655410insertion1nstd207human GRCh38 chr17: 35,133,653-35,133,653 , GRCh37.p13 chr17: 33,460,672-33,460,672 NLE1
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