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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6837978copy number variation1nstd229human GRCh38 chr7: 39,815,544-39,999,163 , GRCh37.p13 chr7: 39,855,143-40,038,762 SSBP3P1, LOC100422519, 5 more genes
    nsv6834393copy number variation1nstd229human GRCh38 chr7: 38,944,248-39,960,814 , GRCh37.p13 chr7: 38,983,848-40,000,413 LOC100422519, LOC646999, 21 more genes
    nsv6830646copy number variation1nstd229human GRCh38 chr7: 39,656,501-41,139,000 , GRCh37.p13 chr7: 39,696,100-41,178,598 RALA, LOC105375242, 22 more genes
    nsv6823172copy number variation1nstd229human GRCh38 chr7: 39,756,607-39,988,428 , GRCh37.p13 chr7: 39,796,206-40,028,027 RN7SL496P, RWDD4P2, 8 more genes
    nsv6820233copy number variation1nstd229human GRCh38 chr7: 39,729,872-40,075,794 , GRCh37.p13 chr7: 39,769,471-40,115,393 RWDD4P2, CICP22, 8 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
    nsv6631947copy number variation1nstd224human GRCh37 chr7: 39,623,495-40,037,248 , GRCh38.p12 chr7: 39,583,896-39,997,649 YAE1, SSBP3P1, 12 more genes
    nsv6611127copy number variation1nstd223human GRCh38 chr7: 39,701,308-39,934,989 , GRCh37.p13 chr7: 39,740,907-39,974,588 CICP22, LOC100422519, 7 more genes
    nsv6609203copy number variation1nstd223human GRCh38 chr7: 39,827,101-39,838,700 , GRCh37.p13 chr7: 39,866,700-39,878,299 LOC101928688, SSBP3P1, 1 more genes
    nsv6604686copy number variation1nstd223human GRCh38 chr7: 39,729,839-40,075,751 , GRCh37.p13 chr7: 39,769,438-40,115,350 SSBP3P1, LOC100422519, 8 more genes
    nsv6601818copy number variation1nstd223human GRCh38 chr7: 39,825,801-39,869,400 , GRCh37.p13 chr7: 39,865,400-39,908,999 SSBP3P1, LOC100422519, 2 more genes
    nsv6600980copy number variation1nstd223human GRCh38 chr7: 39,832,901-39,833,600 , GRCh37.p13 chr7: 39,872,500-39,873,199 SSBP3P1, LOC100422519, 1 more genes
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312346copy number variation1nstd102humanPathogenic GRCh37 chr7: 39,726,267-42,262,852 , GRCh38.p12 chr7: 39,686,668-42,223,253 HMGN2P30, GLI3, 31 more genes
    nsv6290884copy number variation1nstd102humanUncertain significance GRCh37 chr7: 38,728,844-40,069,964 , GRCh38.p12 chr7: 38,689,244-40,030,365 RALA, POU6F2-AS2, 22 more genes
    nsv6136996copy number variation1nstd213human GRCh37 chr7: 39,760,000-39,970,001 , GRCh38.p12 chr7: 39,720,401-39,930,402 LINC00265, RWDD4P2, 6 more genes
    nsv6136995copy number variation1nstd213human GRCh37 chr7: 39,040,000-48,190,001 , GRCh38.p12 chr7: 39,000,400-48,150,404 ADCY1, AEBP1, 161 more genes
    nsv6135992copy number variation1nstd213human GRCh37 chr7: 39,290,000-48,200,001 , GRCh38.p12 chr7: 39,250,401-48,160,404 PSMA2, RALA, 160 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
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