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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6837979copy number variation1nstd229human GRCh38 chr7: 116,279,327-116,287,099 , GRCh37.p13 chr7: 115,919,381-115,927,153 LOC105375463, LOC102724434
    nsv6831475copy number variation1nstd229human GRCh38 chr7: 110,527,230-117,297,230 , GRCh37.p13 chr7: 110,167,287-116,937,284 IMMP2L, LOC105375466, 66 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
    nsv6631744copy number variation1nstd224human GRCh37 chr7: 115,601,453-115,990,649 , GRCh38.p12 chr7: 115,961,399-116,350,595 TES, LOC105375463, 2 more genes
    nsv6631742copy number variation1nstd224human GRCh37 chr7: 114,672,720-116,358,044 , GRCh38.p12 chr7: 115,032,666-116,717,990 CAV1, COMETT, 15 more genes
    nsv6612182copy number variation1nstd223human GRCh38 chr7: 115,721,815-116,342,646 , GRCh37.p13 chr7: 115,361,869-115,982,700 LOC102724407, LOC105375462, 4 more genes
    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
    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
    nsv6135954copy number variation1nstd213human GRCh37 chr7: 114,370,000-117,780,001 , GRCh38.p12 chr7: 114,729,945-118,139,947 TFEC, TES, 40 more genes
    nsv6135876copy number variation1nstd213human GRCh37 chr7: 115,540,000-116,390,001 , GRCh38.p12 chr7: 115,899,946-116,749,947 CAV1, CAV2, 7 more genes
    nsv6135874copy number variation1nstd213human GRCh37 chr7: 114,410,000-116,840,001 , GRCh38.p12 chr7: 114,769,945-117,199,947 CAV1, ST7-OT3, 27 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
    nsv6135542copy number variation1nstd213human GRCh37 chr7: 115,440,000-115,930,001 , GRCh38.p12 chr7: 115,799,946-116,289,947 TFEC, TES, 2 more genes
    nsv6018460copy number variation1nstd212human GRCh38 chr7: 116,273,239-116,275,045 , GRCh37.p13 chr7: 115,913,293-115,915,099 LOC102724434
    nsv6006792copy number variation1nstd212human GRCh38 chr7: 116,277,111-116,277,629 , GRCh37.p13 chr7: 115,917,165-115,917,683 LOC102724434
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5486079copy number variation1nstd206human GRCh38 chr7: 116,273,240-116,275,045 , GRCh37.p13 chr7: 115,913,294-115,915,099 LOC102724434
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