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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137792copy number variation2nstd102humanBenign, Likely benign GRCh38 chr7: 74,059,907-74,059,960 , GRCh37 chr7: 73,474,237-73,474,290 ELN-AS1, ELN
    nsv5974071inversion1nstd209human GRCh37.p13 chr7|NW_003871064.1: 478,880-2,946,547 , GRCh38 chr7: 72,949,644-75,417,311 , CLDN4, 79 more genes
    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
    nsv5673937copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,150,889-73,604,636 , GRCh38.p12 chr7: 73,736,559-74,190,306 EIF4H, ELN-AS1, 8 more genes
    nsv5673850copy number variation1nstd102humanPathogenic GRCh37 chr7: 73,471,702-73,483,040 , GRCh38.p12 chr7: 74,057,372-74,068,710 ELN, ELN-AS1
    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
    nsv5381725copy number variation1nstd102humanUncertain significance GRCh37 chr7: 73,477,473-73,478,035 , GRCh38.p12 chr7: 74,063,143-74,063,705 ELN
    nsv5370698translocation1nstd200human GRCh38 chr7: 74,066,316-74,066,316 , GRCh38 chr18: 73,234,822-73,234,822 , GRCh37.p13 chr7|NW_003871064.1: 1,595,552-1,595,552 , GRCh37.p13 chr18: 70,902,057-70,902,057 , GRCh37.p13 chr7: 73,480,646-73,480,646 ELN, LINC02864
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4966576copy number variation1nstd200human GRCh38 chr7: 74,066,736-74,067,538 , GRCh37.p13 chr7: 73,481,066-73,481,868 , GRCh37.p13 chr7|NW_003871064.1: 1,595,972-1,596,774 ELN
    nsv4966575copy number variation1nstd200human GRCh38 chr7: 74,055,651-74,058,501 , GRCh37.p13 chr7|NW_003871064.1: 1,584,887-1,587,737 , GRCh37.p13 chr7: 73,469,981-73,472,831 ELN, ELN-AS1
    nsv4966574copy number variation1nstd200human GRCh38 chr7: 74,035,794-74,036,861 , GRCh37.p13 chr7|NW_003871064.1: 1,565,030-1,566,097 , GRCh37.p13 chr7: 73,450,124-73,451,191 ELN
    nsv4811877copy number variation1nstd200human GRCh37 chr7: 73,481,066-73,481,868 , GRCh38.p12 chr7: 74,066,736-74,067,538 ELN
    nsv4811876copy number variation1nstd200human GRCh37 chr7: 73,450,124-73,451,191 , GRCh38.p12 chr7: 74,035,794-74,036,861 ELN
    nsv4769380copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,717,369-74,142,224 , GRCh38.p12 chr7: 73,303,372-74,727,886 CLDN4, MLXIPL, 37 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
    nsv4730256inversion12nstd198human GRCh38 chr7: 72,909,603-75,903,316 , GRCh37.p13 chr7|NW_003871064.1: 438,839-3,432,552 , CLDN4, 86 more genes
    nsv4729646copy number variation1nstd102humanPathogenic GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180 LOC105375346, ABHD11-AS1, 70 more genes
    nsv4729135copy number variation1nstd102humanPathogenic GRCh37 chr7: 72,659,674-74,164,894 , GRCh38.p12 chr7: 73,245,641-74,750,557 CLIP2, ABHD11-AS1, 39 more genes
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