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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094547copy number variation1nstd102humanPathogenic GRCh37 chr15: 62,146,656-64,747,263 , GRCh38.p12 chr15: 61,854,457-64,455,064 C2CD4A, SNX22, 40 more genes
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv6971275copy number variation1nstd229human GRCh38 chr15: 62,220,975-62,849,521 , GRCh37.p13 chr15: 62,513,174-63,141,720 MIR8067, LOC102724938, 8 more genes
    nsv6970297copy number variation1nstd229human GRCh38 chr15: 62,546,387-62,815,465 , GRCh37.p13 chr15: 62,838,586-63,107,664 TLN2, LOC105370855, 1 more genes
    nsv6969232copy number variation1nstd229human GRCh38 chr15: 62,630,387-62,650,100 , GRCh37.p13 chr15: 62,922,586-62,942,299 MGC15885, TLN2
    nsv6967898copy number variation1nstd229human GRCh38 chr15: 62,606,595-62,676,313 , GRCh37.p13 chr15: 62,898,794-62,968,512 MGC15885, TLN2, 1 more genes
    nsv6965321copy number variation1nstd229human GRCh38 chr15: 62,567,655-62,670,217 , GRCh37.p13 chr15: 62,859,854-62,962,416 LOC105370855, TLN2, 1 more genes
    nsv6960684copy number variation1nstd229human GRCh38 chr15: 62,287,754-63,705,691 , GRCh37.p13 chr15: 62,579,953-63,997,890 MIR8067, RPS27L, 21 more genes
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6623275copy number variation1nstd224human GRCh37 chr15: 62,788,601-63,353,451 , GRCh38.p12 chr15: 62,496,402-63,061,252 TPM1, TLN2, 6 more genes
    nsv6507845copy number variation1nstd223human GRCh38 chr15: 62,220,975-62,849,523 , GRCh37.p13 chr15: 62,513,174-63,141,722 MGC15885, HMGN1P26, 8 more genes
    nsv6309631copy number variation1nstd102humanUncertain significance GRCh37 chr15: 62,146,656-63,358,098 , GRCh38.p12 chr15: 61,854,457-63,065,899 HMGN1P26, VPS13C-DT, 17 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv5713172mobile element insertion1nstd211human GRCh38 chr15: 62,643,440-62,643,440 , GRCh37.p13 chr15: 62,935,639-62,935,639 TLN2, MGC15885
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4991944copy number variation1nstd200human GRCh38 chr15: 62,642,014-62,642,102 , GRCh37.p13 chr15: 62,934,213-62,934,301 MGC15885, TLN2
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4849787copy number variation1nstd200human GRCh37 chr15: 62,934,213-62,934,301 , GRCh38.p12 chr15: 62,642,014-62,642,102 TLN2, MGC15885
    nsv4729260copy number variation1nstd102humanUncertain significance GRCh37 chr15: 62,810,728-63,024,932 , GRCh38.p12 chr15: 62,518,529-62,732,733 MGC15885, TLN2, 1 more genes
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