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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054011inversion1nstd229human GRCh37.p13 chr7|NW_003871064.1: 3,515,424-3,653,023 , GRCh38 chr7: 75,986,188-76,123,787 , GRCh37.p13 chr7: 75,615,506-75,753,105 GTF2IP7, RNU6-863P, 5 more genes
    nsv7048437inversion1nstd229human GRCh38 chr7: 75,563,042-76,758,264 , GRCh37.p13 chr7: 75,192,346-75,921,852 , GRCh37.p13 chr7|NW_003871064.1: 3,092,278-3,821,770 MIR4651, LINC03009, 26 more genes
    nsv7047526inversion1nstd229human GRCh38 chr7: 75,517,295-76,841,197 , GRCh37.p13 chr7|NW_003871064.1: 3,046,531-3,821,770 , GRCh37.p13 chr7: 75,146,621-75,921,852 CCL24, PMS2P3, 27 more genes
    nsv7045569inversion1nstd229human GRCh37.p13 chr7|NW_003871064.1: 3,480,846-3,653,174 , GRCh38 chr7: 75,951,610-76,123,938 , GRCh37.p13 chr7: 75,580,928-75,753,256 TMEM120A, GTF2IP7, 5 more genes
    nsv7040782inversion1nstd229human GRCh38 chr7: 75,606,397-76,592,714 , GRCh37.p13 chr7: 75,235,715-75,921,852 , GRCh37.p13 chr7|NW_003871064.1: 3,135,633-3,821,770 DTX2, ZP3, 25 more genes
    nsv7039656inversion1nstd229human GRCh38 chr7: 75,704,904-77,508,509 , GRCh37.p13 chr7: 75,921,853-77,137,826 HSPB1, FAM185BP, 45 more genes
    nsv6836572copy number variation1nstd229human GRCh38 chr7: 76,107,993-76,114,147 , GRCh37.p13 chr7: 75,737,311-75,743,465 , GRCh37.p13 chr7|NW_003871064.1: 3,637,229-3,643,383 LOC645324, GTF2IP7
    nsv6818709copy number variation1nstd229human GRCh38 chr7: 74,993,422-78,510,839 , GRCh37.p13 chr7: 75,921,853-78,140,156 TMEM120A, LOC105375359, 75 more genes
    nsv6636822copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 75,085,014-76,007,380 , GRCh38.p12 chr7: 75,455,741-76,378,063 HIP1, HSPB1, 21 more genes
    nsv6636639copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,091,880-75,951,903 , GRCh38.p12 chr7: 75,462,615-76,322,586 LOC100129130, PMS2P3, 20 more genes
    nsv6636453copy number variation1nstd102humanUncertain significance GRCh37 chr7: 75,146,858-75,995,207 , GRCh38.p12 chr7: 75,517,532-76,365,890 MIR4651, CCL26, 19 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632437copy number variation1nstd224human GRCh37 chr7: 75,163,169-76,254,965 , GRCh38.p12 chr7: 75,533,848-76,625,648 HIP1, MDH2, 26 more genes
    nsv6612757copy number variation1nstd223human GRCh37.p13 chr7|NW_003871064.1: 3,576,481-3,719,178 , GRCh38 chr7: 76,047,245-76,189,942 , GRCh37.p13 chr7: 75,676,563-75,819,260 MDH2, STYXL1, 5 more genes
    nsv6607198copy number variation1nstd223human GRCh38 chr7: 75,354,101-76,443,000 , GRCh37.p13 chr7: 74,983,342-75,921,852 , GRCh37.p13 chr7|NW_003871064.1: 2,883,337-3,821,770 ZP3, LOC645324, 28 more genes
    nsv6575132inversion1nstd223human GRCh38 chr7: 76,090,545-76,090,964 , GRCh37.p13 chr7|NW_003871064.1: 3,619,781-3,620,200 , GRCh37.p13 chr7: 75,719,863-75,720,282 GTF2IP7
    nsv6575018inversion1nstd223human GRCh38 chr7: 75,754,131-76,110,069 , GRCh37.p13 chr7|NW_003871064.1: 3,283,367-3,639,305 , GRCh37.p13 chr7: 75,383,449-75,739,387 POR, LOC100129130, 11 more genes
    nsv6574338inversion1nstd223human GRCh38 chr7: 76,102,933-76,103,609 , GRCh37.p13 chr7|NW_003871064.1: 3,632,169-3,632,845 , GRCh37.p13 chr7: 75,732,251-75,732,927 GTF2IP7
    nsv6572498inversion1nstd223human GRCh38 chr7: 75,704,918-77,511,682 , GRCh37.p13 chr7: 75,921,853-77,140,999 LOC645324, FDPSP2, 45 more genes
    nsv6566376inversion1nstd223human GRCh38 chr7: 76,090,451-76,091,267 , GRCh37.p13 chr7: 75,719,769-75,720,585 , GRCh37.p13 chr7|NW_003871064.1: 3,619,687-3,620,503 GTF2IP7
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