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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6833664copy number variation1nstd229human GRCh38 chr7: 117,743,324-119,522,444 , GRCh37.p13 chr7: 117,383,378-119,162,498 GTF3AP6, LOC648442, 9 more genes
    nsv6832306copy number variation1nstd229human GRCh38 chr7: 117,735,001-118,626,000 , GRCh37.p13 chr7: 117,375,055-118,266,054 LOC105375472, CTTNBP2, 7 more genes
    nsv6831931copy number variation1nstd229human GRCh38 chr7: 118,005,965-119,442,817 , GRCh37.p13 chr7: 117,646,019-119,082,871 LOC102724495, LOC105375472, 8 more genes
    nsv6824980copy number variation1nstd229human GRCh38 chr7: 118,200,749-118,200,943 , GRCh37.p13 chr7: 117,840,803-117,840,997 LSM8
    nsv6820380copy number variation1nstd229human GRCh38 chr7: 118,196,801-118,203,600 , GRCh37.p13 chr7: 117,836,855-117,843,654 LSM8
    nsv6636199copy number variation1nstd102humanUncertain significance GRCh37 chr7: 117,768,606-118,009,488 , GRCh38.p12 chr7: 118,128,552-118,369,434 LOC105375470, ANKRD7, 2 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
    nsv6613890copy number variation1nstd223human GRCh38 chr7: 118,185,701-118,187,600 , GRCh37.p13 chr7: 117,825,755-117,827,654 LSM8
    nsv6611731copy number variation1nstd223human GRCh38 chr7: 118,147,601-118,234,750 , GRCh37.p13 chr7: 117,787,655-117,874,804 LOC105375470, ANKRD7, 1 more genes
    nsv6609050copy number variation1nstd223human GRCh38 chr7: 118,124,400-118,188,092 , GRCh37.p13 chr7: 117,764,454-117,828,146 LOC105375470, LSM8
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6269886copy number variation1nstd214human GRCh38 chr7: 118,182,193-118,182,323 , GRCh37.p13 chr7: 117,822,247-117,822,377 LSM8, LOC105375470
    nsv6136544copy number variation1nstd213human GRCh37 chr7: 117,830,000-118,330,001 , GRCh38.p12 chr7: 118,189,946-118,689,947 LSM8, ANKRD7, 5 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135879copy number variation1nstd213human GRCh37 chr7: 117,650,000-118,190,001 , GRCh38.p12 chr7: 118,009,946-118,549,947 LSM8, ANKRD7, 6 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv6135544copy number variation1nstd213human GRCh37 chr7: 117,090,000-118,860,001 , GRCh38.p12 chr7: 117,449,946-119,219,947 LSM8, CTTNBP2, 13 more genes
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