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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148157copy number variation1nstd102humanPathogenic GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396 OR7E84P, FAM193A, 764 more genes
    nsv6732761copy number variation1nstd229human GRCh38 chr4: 53,602,851-53,608,613 , GRCh37.p13 chr4: 54,469,018-54,474,780 LNX1, LNX1-AS2
    nsv6723611copy number variation1nstd229human GRCh38 chr4: 53,596,296-53,625,070 , GRCh37.p13 chr4: 54,462,463-54,491,237 LNX1-AS2, LNX1
    nsv6637063copy number variation1nstd102humanUncertain significance GRCh37 chr4: 52,685,980-59,272,025 , GRCh38.p12 chr4: 51,819,814-58,405,859 SPINK2, RN7SL492P, 100 more genes
    nsv6395002copy number variation1nstd223human GRCh38 chr4: 53,605,162-53,674,409 , GRCh37.p13 chr4: 54,471,329-54,540,576 LNX1, LNX1-AS2
    nsv6315421copy number variation1nstd102humanPathogenic GRCh37 chr4: 53,688,710-56,491,447 , GRCh38.p12 chr4: 52,822,543-55,625,280 METTL5P3, RPL38P3, 38 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291206copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,685,685-58,104,722 , GRCh38.p12 chr4: 51,819,519-57,238,556 SRD5A3, DCUN1D4, 96 more genes
    nsv6244075mobile element insertion1nstd215human GRCh38 chr4: 53,595,784-53,595,784 , GRCh37.p13 chr4: 54,461,951-54,461,951 LNX1, LNX1-AS2
    nsv6135591copy number variation1nstd213human GRCh37 chr4: 54,250,000-54,540,001 , GRCh38.p12 chr4: 53,383,833-53,673,834 FIP1L1, LNX1, 3 more genes
    nsv5892144copy number variation1nstd209human GRCh38 chr4: 53,602,844-53,608,611 , GRCh37.p13 chr4: 54,469,011-54,474,778 LNX1, LNX1-AS2
    nsv5839673copy number variation1nstd209human GRCh38 chr4: 53,604,991-53,606,685 , GRCh37.p13 chr4: 54,471,158-54,472,852 LNX1, LNX1-AS2
    nsv5839365copy number variation1nstd209human GRCh38 chr4: 53,602,841-53,608,685 , GRCh37.p13 chr4: 54,469,008-54,474,852 LNX1-AS2, LNX1
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5463976copy number variation1nstd206human GRCh38 chr4: 53,602,844-53,608,612 , GRCh37.p13 chr4: 54,469,011-54,474,779 LNX1-AS2, LNX1
    nsv5311475copy number variation1nstd204human GRCh37.p13 chr4: 54,457,810-54,462,976 , GRCh38.p13 chr4: 53,591,643-53,596,809 LNX1, LNX1-AS2
    nsv5236293copy number variation1nstd204human GRCh38.p13 chr4: 53,591,656-53,597,348 , GRCh37.p13 chr4: 54,457,823-54,463,515 LNX1-AS2, LNX1
    nsv5039232inversion1nstd200human GRCh38 chr4: 9,660,225-57,055,279 , GRCh37.p13 chr4: 9,661,849-57,921,445 , KRT18P63, 533 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925615copy number variation1nstd200human GRCh38 chr4: 53,605,162-53,674,409 , GRCh37.p13 chr4: 54,471,329-54,540,576 LNX1, LNX1-AS2
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