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Items: 1 to 20 of 623

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146987insertion1nstd232human GRCh37.p13 chr2: 157,077,125-157,077,125 , GRCh38.p12 chr2: 156,220,613-156,220,613 LINC01876
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7052508inversion1nstd229human GRCh38 chr2: 156,045,377-156,051,912 , GRCh37.p13 chr2: 156,901,889-156,908,424 LINC01876
    nsv7050082inversion1nstd229human GRCh38 chr2: 154,880,025-156,722,310 , GRCh37.p13 chr2: 155,736,537-157,578,822 LOC105373703, LOC107985828, 25 more genes
    nsv7048490inversion1nstd229human GRCh38 chr2: 156,054,444-158,055,095 , GRCh37.p13 chr2: 156,910,956-158,911,607 CYTIP, LINC01876, 23 more genes
    nsv7047988inversion1nstd229human GRCh38 chr2: 156,139,085-156,139,165 , GRCh37.p13 chr2: 156,995,597-156,995,677 LINC01876
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6697935copy number variation1nstd229human GRCh38 chr2: 156,187,860-156,195,982 , GRCh37.p13 chr2: 157,044,372-157,052,494 LINC01876
    nsv6697500copy number variation1nstd229human GRCh38 chr2: 156,128,598-156,133,053 , GRCh37.p13 chr2: 156,985,110-156,989,565 LINC01876
    nsv6696752copy number variation1nstd229human GRCh38 chr2: 155,870,119-156,198,989 , GRCh37.p13 chr2: 156,726,631-157,055,501 LOC105373703, LINC01876, 1 more genes
    nsv6694921copy number variation1nstd229human GRCh38 chr2: 156,224,793-156,269,308 , GRCh37.p13 chr2: 157,081,305-157,125,820 LINC01876
    nsv6694175copy number variation1nstd229human GRCh38 chr2: 156,128,937-156,132,812 , GRCh37.p13 chr2: 156,985,449-156,989,324 LINC01876
    nsv6694174copy number variation1nstd229human GRCh38 chr2: 156,194,601-156,297,300 , GRCh37.p13 chr2: 157,051,113-157,153,812 LINC01876
    nsv6691769copy number variation1nstd229human GRCh38 chr2: 156,205,001-156,209,000 , GRCh37.p13 chr2: 157,061,513-157,065,512 LINC01876
    nsv6691718copy number variation1nstd229human GRCh38 chr2: 156,095,996-156,097,477 , GRCh37.p13 chr2: 156,952,508-156,953,989 LINC01876
    nsv6689954copy number variation1nstd229human GRCh38 chr2: 156,213,024-156,216,439 , GRCh37.p13 chr2: 157,069,536-157,072,951 LINC01876
    nsv6689912copy number variation1nstd229human GRCh38 chr2: 156,001,457-156,033,972 , GRCh37.p13 chr2: 156,857,969-156,890,484 LINC01876, HEBP2P1
    nsv6689521copy number variation1nstd229human GRCh38 chr2: 156,130,233-156,130,261 , GRCh37.p13 chr2: 156,986,745-156,986,773 LINC01876
    nsv6689297copy number variation1nstd229human GRCh38 chr2: 156,220,613-156,220,822 , GRCh37.p13 chr2: 157,077,125-157,077,334 LINC01876
    nsv6688174copy number variation1nstd229human GRCh38 chr2: 156,031,470-156,036,690 , GRCh37.p13 chr2: 156,887,982-156,893,202 HEBP2P1, LINC01876
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