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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    nsv5921888copy number variation1nstd209human GRCh38 chr7: 74,241,026-74,241,705 , GRCh37.p13 chr7|NW_003871064.1: 1,770,262-1,770,941 , GRCh37.p13 chr7: 73,655,356-73,656,035 RFC2
    nsv5921774copy number variation1nstd209human GRCh38 chr7: 74,245,723-74,246,205 , GRCh37.p13 chr7: 73,660,053-73,660,535 , GRCh37.p13 chr7|NW_003871064.1: 1,774,959-1,775,441 RFC2
    nsv5918891copy number variation1nstd209human GRCh38 chr7: 71,592,506-75,175,408 , GRCh37.p13 chr7|NW_003871064.1: 1-2,704,644 , GRCh37.p13 chr7: 71,935,722-74,527,751 , SPDYE10, 78 more genes
    nsv5915223copy number variation1nstd209human GRCh38 chr7: 74,235,257-74,235,401 , GRCh37.p13 chr7|NW_003871064.1: 1,764,493-1,764,637 , GRCh37.p13 chr7: 73,649,587-73,649,731 RFC2
    nsv5666565inversion1nstd207human GRCh38 chr7: 73,113,990-75,217,887 , GRCh37.p13 chr7|NW_003871064.1: 643,226-2,747,123 , CLDN4, 57 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487881copy number variation1nstd206human GRCh38 chr7: 74,241,026-74,241,706 , GRCh37.p13 chr7: 73,655,356-73,656,036 , GRCh37.p13 chr7|NW_003871064.1: 1,770,262-1,770,942 RFC2
    nsv5486332copy number variation1nstd206human GRCh38 chr7: 74,244,644-74,245,310 , GRCh37.p13 chr7|NW_003871064.1: 1,773,880-1,774,546 , GRCh37.p13 chr7: 73,658,974-73,659,640 RFC2
    nsv5230591copy number variation1nstd204human GRCh38.p13 chr7: 74,232,789-74,234,812 , GRCh37.p13 chr7|NW_003871064.1: 1,762,025-1,764,048 , GRCh37.p13 chr7: 73,647,119-73,649,142 RFC2
    nsv5190314mobile element insertion1nstd203human GRCh38 chr7: 74,250,452-74,250,452 , GRCh37.p13 chr7|NW_003871064.1: 1,779,688-1,779,688 , GRCh37.p13 chr7: 73,664,782-73,664,782 RFC2
    nsv5188246mobile element insertion1nstd203human GRCh38 chr7: 74,250,448-74,250,452 , GRCh37.p13 chr7|NW_003871064.1: 1,779,684-1,779,688 , GRCh37.p13 chr7: 73,664,778-73,664,782 RFC2
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966590copy number variation1nstd200human GRCh38 chr7: 74,254,565-74,254,739 , GRCh37.p13 chr7: 73,668,895-73,669,069 , GRCh37.p13 chr7|NW_003871064.1: 1,783,801-1,783,975 RFC2
    nsv4966589copy number variation1nstd200human GRCh38 chr7: 74,245,879-74,249,269 , GRCh37.p13 chr7|NW_003871064.1: 1,775,115-1,778,505 , GRCh37.p13 chr7: 73,660,209-73,663,599 RFC2
    nsv4966588copy number variation1nstd200human GRCh38 chr7: 74,241,026-74,241,706 , GRCh37.p13 chr7: 73,655,356-73,656,036 , GRCh37.p13 chr7|NW_003871064.1: 1,770,262-1,770,942 RFC2
    nsv4966587copy number variation1nstd200human GRCh38 chr7: 74,233,822-74,234,696 , GRCh37.p13 chr7|NW_003871064.1: 1,763,058-1,763,932 , GRCh37.p13 chr7: 73,648,152-73,649,026 RFC2
    nsv4966586copy number variation1nstd200human GRCh38 chr7: 74,233,073-74,239,623 , GRCh37.p13 chr7|NW_003871064.1: 1,762,309-1,768,859 , GRCh37.p13 chr7: 73,647,403-73,653,953 RFC2
    nsv4954052copy number variation1nstd200human GRCh38 chr7: 74,244,615-74,245,306 , GRCh37.p13 chr7: 73,658,945-73,659,636 , GRCh37.p13 chr7|NW_003871064.1: 1,773,851-1,774,542 RFC2
    nsv4811897copy number variation1nstd200human GRCh37 chr7: 73,665,922-73,666,487 , GRCh38.p12 chr7: 74,251,592-74,252,157 RFC2
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