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Items: 1 to 20 of 774

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7075519inversion1nstd229human GRCh38 chr9: 69,476,392-69,476,458 , GRCh37.p13 chr9: 72,091,308-72,091,374 APBA1
    nsv7064688inversion1nstd229human GRCh38 chr9: 69,453,113-69,486,473 , GRCh37.p13 chr9: 72,068,029-72,101,389 APBA1
    nsv7059369inversion1nstd229human GRCh38 chr9: 69,068,268-69,425,843 , GRCh37.p13 chr9: 71,683,184-72,040,759 TJP2, BANCR, 3 more genes
    nsv6877824copy number variation1nstd229human GRCh38 chr9: 69,624,807-69,630,491 , GRCh37.p13 chr9: 72,239,723-72,245,407 APBA1
    nsv6876436copy number variation1nstd229human GRCh38 chr9: 69,579,060-69,579,162 , GRCh37.p13 chr9: 72,193,976-72,194,078 APBA1
    nsv6874722copy number variation1nstd229human GRCh38 chr9: 69,539,597-69,539,678 , GRCh37.p13 chr9: 72,154,513-72,154,594 APBA1
    nsv6871598copy number variation1nstd229human GRCh38 chr9: 69,540,391-69,546,272 , GRCh37.p13 chr9: 72,155,307-72,161,188 APBA1
    nsv6871520copy number variation1nstd229human GRCh38 chr9: 69,477,501-69,510,000 , GRCh37.p13 chr9: 72,092,417-72,124,916 APBA1
    nsv6871251copy number variation1nstd229human GRCh38 chr9: 69,471,756-69,471,970 , GRCh37.p13 chr9: 72,086,672-72,086,886 APBA1
    nsv6870645copy number variation1nstd229human GRCh38 chr9: 69,232,258-69,656,226 , GRCh37.p13 chr9: 71,847,174-72,271,142 BANCR, ENTREP1, 2 more genes
    nsv6870076copy number variation1nstd229human GRCh38 chr9: 69,351,612-69,433,403 , GRCh37.p13 chr9: 71,966,528-72,048,319 APBA1, ENTREP1
    nsv6866946copy number variation1nstd229human GRCh38 chr9: 69,487,025-69,498,583 , GRCh37.p13 chr9: 72,101,941-72,113,499 APBA1
    nsv6865242copy number variation1nstd229human GRCh38 chr9: 69,661,158-69,787,043 , GRCh37.p13 chr9: 72,276,074-72,401,959 APBA1, LOC105376076, 1 more genes
    nsv6865067copy number variation1nstd229human GRCh38 chr9: 69,379,905-69,564,293 , GRCh37.p13 chr9: 71,994,821-72,179,209 APBA1, ENTREP1
    nsv6864267copy number variation1nstd229human GRCh38 chr9: 69,559,268-69,561,779 , GRCh37.p13 chr9: 72,174,184-72,176,695 APBA1
    nsv6863062copy number variation1nstd229human GRCh38 chr9: 69,419,262-69,430,578 , GRCh37.p13 chr9: 72,034,178-72,045,494 APBA1
    nsv6861879copy number variation1nstd229human GRCh38 chr9: 69,448,255-69,452,083 , GRCh37.p13 chr9: 72,063,171-72,066,999 APBA1
    nsv6861789copy number variation1nstd229human GRCh38 chr9: 69,535,915-69,538,114 , GRCh37.p13 chr9: 72,150,831-72,153,030 APBA1
    nsv6861495copy number variation1nstd229human GRCh38 chr9: 69,446,434-69,446,549 , GRCh37.p13 chr9: 72,061,350-72,061,465 APBA1
    nsv6860903copy number variation1nstd229human GRCh38 chr9: 69,555,774-69,561,975 , GRCh37.p13 chr9: 72,170,690-72,176,891 APBA1
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