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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    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
    nsv6836235copy number variation1nstd229human GRCh38 chr7: 75,942,469-75,942,953 , GRCh37.p13 chr7|NW_003871064.1: 3,471,705-3,472,189 , GRCh37.p13 chr7: 75,571,787-75,572,271 POR, SNORA14A
    nsv6835473copy number variation1nstd229human GRCh38 chr7: 75,824,758-75,957,971 , GRCh37.p13 chr7|NW_003871064.1: 3,353,994-3,487,207 , GRCh37.p13 chr7: 75,454,076-75,587,289 MIR4651, RHBDD2, 4 more genes
    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
    nsv6614163copy number variation1nstd223human GRCh37.p13 chr7|NW_003871064.1: 3,364,632-3,486,129 , GRCh38 chr7: 75,835,396-75,956,893 , GRCh37.p13 chr7: 75,464,714-75,586,211 POR, RHBDD2, 4 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
    nsv6602803copy number variation1nstd223human GRCh38 chr7: 75,942,460-75,942,953 , GRCh37.p13 chr7|NW_003871064.1: 3,471,696-3,472,189 , GRCh37.p13 chr7: 75,571,778-75,572,271 SNORA14A, POR
    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
    nsv6572498inversion1nstd223human GRCh38 chr7: 75,704,918-77,511,682 , GRCh37.p13 chr7: 75,921,853-77,140,999 LOC645324, FDPSP2, 45 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6290688copy number variation1nstd102humanPathogenic GRCh38 chr7: 75,058,300-79,083,658 , GRCh37.p13 chr7: 75,921,853-78,712,974 GTF2IP1, TMEM60, 76 more genes
    nsv6142543copy number variation1nstd206human GRCh38 chr7: 75,942,469-75,943,039 , GRCh37.p13 chr7|NW_003871064.1: 3,471,705-3,472,275 , GRCh37.p13 chr7: 75,571,787-75,572,357 POR, SNORA14A
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