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Items: 1 to 20 of 547

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143782insertion1nstd232human GRCh37.p13 chr2: 102,503,697-102,503,697 , GRCh38.p12 chr2: 101,887,235-101,887,235 MAP4K4
    nsv7054692inversion1nstd229human GRCh38 chr2: 101,799,196-101,799,223 , GRCh37.p13 chr2: 102,415,658-102,415,685 MAP4K4
    nsv7053207inversion1nstd229human GRCh38 chr2: 101,821,578-101,821,648 , GRCh37.p13 chr2: 102,438,040-102,438,110 MAP4K4
    nsv7051311inversion1nstd229human GRCh38 chr2: 101,647,680-105,928,217 , GRCh37.p13 chr2: 102,264,142-106,544,673 LOC107985929, SLC9A2, 57 more genes
    nsv7041609inversion1nstd229human GRCh38 chr2: 101,840,216-101,853,311 , GRCh37.p13 chr2: 102,456,678-102,469,773 MAP4K4
    nsv7038126inversion1nstd229human GRCh38 chr2: 101,771,613-101,771,743 , GRCh37.p13 chr2: 102,388,075-102,388,205 MAP4K4
    nsv6697213copy number variation1nstd229human GRCh38 chr2: 101,552,301-101,698,500 , GRCh37.p13 chr2: 102,168,763-102,314,962 MAP4K4, LOC105373514
    nsv6696800copy number variation1nstd229human GRCh38 chr2: 101,727,279-101,753,400 , GRCh37.p13 chr2: 102,343,741-102,369,862 MAP4K4
    nsv6695770copy number variation1nstd229human GRCh38 chr2: 101,102,526-102,065,468 , GRCh37.p13 chr2: 101,718,988-102,681,928 LOC107985789, PRCPP1, 17 more genes
    nsv6690889copy number variation1nstd229human GRCh38 chr2: 101,860,744-101,909,552 , GRCh37.p13 chr2: 102,477,206-102,526,014 MAP4K4
    nsv6690558copy number variation1nstd229human GRCh38 chr2: 101,765,921-101,777,140 , GRCh37.p13 chr2: 102,382,383-102,393,602 MAP4K4
    nsv6687279copy number variation1nstd229human GRCh38 chr2: 101,279,320-101,725,723 , GRCh37.p13 chr2: 101,895,782-102,342,185 MIR5696, LOC105373512, 9 more genes
    nsv6685797copy number variation1nstd229human GRCh38 chr2: 101,759,031-101,779,276 , GRCh37.p13 chr2: 102,375,493-102,395,738 MAP4K4
    nsv6682919copy number variation1nstd229human GRCh38 chr2: 101,578,101-101,699,100 , GRCh37.p13 chr2: 102,194,563-102,315,562 MAP4K4
    nsv6681728copy number variation1nstd229human GRCh38 chr2: 101,704,801-101,707,000 , GRCh37.p13 chr2: 102,321,263-102,323,462 MAP4K4
    nsv6681664copy number variation1nstd229human GRCh38 chr2: 101,777,349-101,784,979 , GRCh37.p13 chr2: 102,393,811-102,401,441 MAP4K4
    nsv6680627copy number variation1nstd229human GRCh38 chr2: 101,740,153-101,740,453 , GRCh37.p13 chr2: 102,356,615-102,356,915 MAP4K4
    nsv6679286copy number variation1nstd229human GRCh38 chr2: 101,748,588-101,760,784 , GRCh37.p13 chr2: 102,365,050-102,377,246 MAP4K4
    nsv6679058copy number variation1nstd229human GRCh38 chr2: 101,850,915-101,850,953 , GRCh37.p13 chr2: 102,467,377-102,467,415 MAP4K4
    nsv6679055copy number variation1nstd229human GRCh38 chr2: 101,801,193-101,920,076 , GRCh37.p13 chr2: 102,417,655-102,536,538 MAP4K4
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