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Items: 1 to 20 of 445

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6124217insertion1nstd186human GRCh37 chr5: 29,069,317-29,069,317 , GRCh38.p12 chr5: 29,069,210-29,069,210 , GRCh38.p12 chr5|NW_003571036.1: 32,683-32,683 LOC101929645
    nsv5342193translocation1nstd200human GRCh37 chr5: 29,184,088-29,184,088 , GRCh37 chr5: 29,184,338-29,184,338 , GRCh38.p12 chr5|NW_003571036.1: 156,614-156,614 , GRCh38.p12 chr5|NW_003571036.1: 156,364-156,364 , GRCh38.p12 chr5: 29,183,981-29,183,981 , GRCh38.p12 chr5: 29,184,231-29,184,231 0
    nsv4802329copy number variation1nstd200human GRCh37 chr5: 29,235,824-29,257,698 , GRCh38.p12 chr5: 29,235,717-29,257,591 , GRCh38.p12 chr5|NW_003571036.1: 208,100-226,852 0
    nsv4802327copy number variation1nstd200human GRCh37 chr5: 29,115,933-29,117,272 , GRCh38.p12 chr5: 29,115,826-29,117,165 , GRCh38.p12 chr5|NW_003571036.1: 88,209-89,548 LOC105374699
    nsv4802326copy number variation1nstd200human GRCh37 chr5: 29,110,001-29,110,060 , GRCh38.p12 chr5|NW_003571036.1: 82,276-82,335 , GRCh38.p12 chr5: 29,109,894-29,109,953 LOC105374699
    nsv4802325copy number variation1nstd200human GRCh37 chr5: 29,045,172-29,045,924 , GRCh38.p12 chr5: 29,045,065-29,045,817 , GRCh38.p12 chr5|NW_003571036.1: 8,582-9,334
    nsv4723446insertion1nstd186human GRCh37 chr5: 29,069,930-29,069,930 , GRCh38.p12 chr5: 29,069,823-29,069,823 , GRCh38.p12 chr5|NW_003571036.1: 42,214-42,214 LOC101929645
    nsv4593056copy number variation1nstd183human GRCh37 chr5: 29,186,531-29,206,379 , GRCh38.p12 chr5: 29,186,424-29,206,272 , GRCh38.p12 chr5|NW_003571036.1: 158,807-178,655 0
    nsv4593055copy number variation1nstd183human GRCh37 chr5: 29,077,782-29,082,580 , GRCh38.p12 chr5: 29,077,675-29,082,473 , GRCh38.p12 chr5|NW_003571036.1: 50,067-54,861 LOC105374699
    nsv4593054copy number variation1nstd183human GRCh37 chr5: 29,046,862-29,117,411 , GRCh38.p12 chr5|NW_003571036.1: 10,272-89,687 , GRCh38.p12 chr5: 29,046,755-29,117,304 , LOC101929645, 2 more genes
    nsv4593053copy number variation1nstd183human GRCh37 chr5: 28,936,207-29,148,873 , GRCh38.p12 chr5: 28,936,100-29,148,766 , GRCh38.p12 chr5|NW_003571036.1: 1-121,149 , SUCLG2P4, 4 more genes
    nsv4591063copy number variation1nstd183human GRCh37 chr5: 29,034,294-29,044,730 , GRCh38.p12 chr5: 29,034,187-29,044,623 , GRCh38.p12 chr5|NW_003571036.1: 1-8,141
    nsv4590939copy number variation1nstd183human GRCh37 chr5: 29,076,472-29,195,987 , GRCh38.p12 chr5: 29,076,365-29,195,880 , GRCh38.p12 chr5|NW_003571036.1: 48,757-168,263 LOC105374699, LINC02109, 1 more genes
    nsv4568083mobile element insertion1nstd166human GRCh37.p13 chr5: 29,054,583-29,054,583 , GRCh38.p12 chr5: 29,054,476-29,054,476 , GRCh38.p12 chr5|NW_003571036.1: 17,971-17,971
    nsv4559601inversion1nstd166human GRCh37.p13 chr5: 29,209,760-29,226,706 , GRCh38.p12 chr5|NW_003571036.1: 182,036-198,982 , GRCh38.p12 chr5: 29,209,653-29,226,599 0
    nsv4549460insertion1nstd166human GRCh37.p13 chr5: 29,149,776-29,149,776 , GRCh38.p12 chr5|NW_003571036.1: 122,052-122,052 , GRCh38.p12 chr5: 29,149,669-29,149,669 LINC02109
    nsv4548865insertion1nstd166human GRCh37.p13 chr5: 29,153,284-29,153,284 , GRCh38.p12 chr5|NW_003571036.1: 125,560-125,560 , GRCh38.p12 chr5: 29,153,177-29,153,177 LINC02109
    nsv4523040copy number variation1nstd166human GRCh37.p13 chr5: 29,184,088-29,184,338 , GRCh38.p12 chr5: 29,183,981-29,184,231 , GRCh38.p12 chr5|NW_003571036.1: 156,364-156,614 0
    nsv4478086mobile element insertion1nstd166human GRCh37.p13 chr5: 29,124,854-29,124,854 , GRCh38.p12 chr5: 29,124,747-29,124,747 , GRCh38.p12 chr5|NW_003571036.1: 97,130-97,130 LOC105374699
    nsv4477964mobile element insertion1nstd166human GRCh37.p13 chr5: 29,248,415-29,248,415 , GRCh38.p12 chr5|NW_003571036.1: 220,691-220,691 , GRCh38.p12 chr5: 29,248,308-29,248,308 0
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