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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 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
    nsv6603292copy number variation1nstd223human GRCh38 chr7: 75,414,001-75,417,400 , GRCh37.p13 chr7: 75,043,279-75,046,683 , GRCh37.p13 chr7|NW_003871064.1: 2,943,237-2,946,636 NSUN5P1, POM121C
    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
    nsv6142851copy number variation1nstd206human GRCh38 chr7: 75,406,779-75,417,500 , GRCh37.p13 chr7|NW_003871064.1: 2,936,015-2,946,736 , GRCh37.p13 chr7: 75,036,063-75,046,783 POM121C, NSUN5P1
    nsv6142646copy number variation1nstd206human GRCh37.p13 chr7|NW_003871064.1: 2,931,336-2,970,015 , GRCh38 chr7: 75,402,100-75,440,779 , GRCh37.p13 chr7: 75,031,383-75,070,057 NSUN5P1, TRIM73, 1 more genes
    nsv6137011copy number variation1nstd213human GRCh37 chr7: 75,030,000-76,100,001 , GRCh38.p12 chr7: 75,400,716-76,470,684 HIP1, MDH2, 27 more genes
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5863878copy number variation1nstd209human GRCh38 chr7: 75,415,882-75,427,168 , GRCh37.p13 chr7|NW_003871064.1: 2,945,118-2,956,404 , GRCh37.p13 chr7: 75,045,160-75,056,450 POM121C, NSUN5P1
    nsv5862671copy number variation1nstd209human GRCh38 chr7: 75,414,419-75,417,633 , GRCh37.p13 chr7|NW_003871064.1: 2,943,655-2,946,869 , GRCh37.p13 chr7: 75,043,697-75,046,916 POM121C, NSUN5P1
    nsv5854452copy number variation1nstd209human GRCh38 chr7: 75,414,420-75,420,493 , GRCh37.p13 chr7: 75,043,698-75,049,776 , GRCh37.p13 chr7|NW_003871064.1: 2,943,656-2,949,729 POM121C, NSUN5P1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5234255copy number variation1nstd204human GRCh38.p13 chr7: 75,417,101-75,422,400 , GRCh37.p13 chr7|NW_003871064.1: 2,946,337-2,951,636 , GRCh37.p13 chr7: 75,046,384-75,051,683 POM121C, NSUN5P1
    nsv5232728copy number variation1nstd204human GRCh38.p13 chr7: 75,415,131-75,417,184 , GRCh37.p13 chr7|NW_003871064.1: 2,944,367-2,946,420 , GRCh37.p13 chr7: 75,044,409-75,046,467 POM121C, NSUN5P1
    nsv5231344copy number variation1nstd204human GRCh38.p13 chr7: 75,417,135-75,425,932 , GRCh37.p13 chr7: 75,046,418-75,055,214 , GRCh37.p13 chr7|NW_003871064.1: 2,946,371-2,955,168 NSUN5P1, POM121C
    nsv5226395copy number variation1nstd204human GRCh38.p13 chr7: 75,414,419-75,417,033 , GRCh37.p13 chr7: 75,043,697-75,046,312 , GRCh37.p13 chr7|NW_003871064.1: 2,943,655-2,946,269 POM121C, NSUN5P1
    nsv5224278copy number variation1nstd204human GRCh38.p13 chr7: 75,413,001-75,417,200 , GRCh37.p13 chr7: 75,042,279-75,046,483 , GRCh37.p13 chr7|NW_003871064.1: 2,942,237-2,946,436 POM121C, NSUN5P1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
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