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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096682copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 132,438,675-132,441,126 , GRCh38.p12 chr3: 132,719,831-132,722,282 NPHP3, NPHP3-AS1, 1 more genes
    nsv7096441copy number variation1nstd102humanPathogenic GRCh37 chr3: 132,410,016-132,411,682 , GRCh38.p12 chr3: 132,691,172-132,692,838 NPHP3-ACAD11, NPHP3
    nsv7052094inversion1nstd229human GRCh38 chr3: 132,609,279-139,052,095 , GRCh37.p13 chr3: 132,328,123-138,770,937 RNU6-789P, UBA5, 98 more genes
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv6735358copy number variation1nstd229human GRCh38 chr3: 132,603,776-132,991,813 , GRCh37.p13 chr3: 132,322,620-132,710,657 HSPA8P19, NPHP3, 5 more genes
    nsv6732892copy number variation1nstd229human GRCh38 chr3: 132,697,698-132,712,079 , GRCh37.p13 chr3: 132,416,542-132,430,923 NPHP3-ACAD11, NPHP3
    nsv6720341copy number variation1nstd229human GRCh38 chr3: 132,678,701-132,681,600 , GRCh37.p13 chr3: 132,397,545-132,400,444 NPHP3-ACAD11, UBA5, 1 more genes
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6636781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,355,551-132,993,069 , GRCh38.p12 chr3: 132,636,707-133,274,225 TMEM108-AS1, TMEM108, 7 more genes
    nsv6636304copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,080,316-132,705,445 , GRCh38.p12 chr3: 132,361,472-132,986,601 UBA5, DNAJC13, 10 more genes
    nsv6634732copy number variation1nstd227human GRCh37 chr3: 132,361,596-132,414,454 , GRCh38.p12 chr3: 132,642,752-132,695,610 NPHP3, UBA5, 3 more genes
    nsv6566356inversion1nstd223human GRCh38 chr3: 132,708,998-132,710,676 , GRCh37.p13 chr3: 132,427,842-132,429,520 NPHP3-ACAD11, NPHP3
    nsv6559124inversion1nstd223human GRCh38 chr3: 132,678,661-132,679,191 , GRCh37.p13 chr3: 132,397,505-132,398,035 NPHP3, UBA5, 1 more genes
    nsv6557474inversion1nstd223human GRCh38 chr3: 132,678,795-132,679,247 , GRCh37.p13 chr3: 132,397,639-132,398,091 NPHP3, UBA5, 1 more genes
    nsv6371675copy number variation1nstd223human GRCh38 chr3: 132,697,698-132,712,076 , GRCh37.p13 chr3: 132,416,542-132,430,920 NPHP3, NPHP3-ACAD11
    nsv6371540copy number variation1nstd223human GRCh38 chr3: 132,603,801-132,991,800 , GRCh37.p13 chr3: 132,322,645-132,710,644 NPHP3, UBA5, 5 more genes
    nsv6359869copy number variation1nstd223human GRCh38 chr3: 132,679,116-132,679,880 , GRCh37.p13 chr3: 132,397,960-132,398,724 NPHP3, NPHP3-ACAD11, 1 more genes
    nsv6311952copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr3: 132,379,382-132,441,199 , GRCh38.p12 chr3: 132,660,538-132,722,355 NPHP3, UBA5, 3 more genes
    nsv6311854copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,407,898-132,411,682 , GRCh38.p12 chr3: 132,689,054-132,692,838 NPHP3, NPHP3-ACAD11
    nsv6311776copy number variation1nstd102humanUncertain significance GRCh37 chr3: 132,413,221-132,415,677 , GRCh38.p12 chr3: 132,694,377-132,696,833 NPHP3, NPHP3-ACAD11
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