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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140074insertion1nstd232human GRCh37.p13 chr17: 16,342,732-16,342,732 , GRCh38.p12 chr17: 16,439,418-16,439,418 SNORD49A, SNHG29, 2 more genes
    nsv7138047insertion1nstd232human GRCh37.p13 chr17: 16,343,018-16,343,018 , GRCh38.p12 chr17: 16,439,704-16,439,704 SNORD49A, SNHG29, 3 more genes
    nsv7073486inversion1nstd229human GRCh38 chr17: 15,622,817-18,740,940 , GRCh37.p13 chr17: 15,526,131-18,644,253 NCOR1, KRT16P6, 129 more genes
    nsv7073439inversion1nstd229human GRCh38 chr17: 15,962,151-19,146,977 , GRCh37.p13 chr17: 15,865,465-19,050,290 RNU6-767P, KRT17P5, 129 more genes
    nsv7066862inversion1nstd229human GRCh38 chr17: 15,664,455-18,717,083 , GRCh37.p13 chr17: 15,567,769-18,620,396 KRT16P6, RPLP1P11, 129 more genes
    nsv7063823inversion1nstd229human GRCh38 chr17: 16,127,666-16,472,211 , GRCh37.p13 chr17: 16,030,980-16,375,525 NCOR1, SNORD163, 13 more genes
    nsv7059660inversion1nstd229human GRCh38 chr17: 16,041,448-17,186,703 , GRCh37.p13 chr17: 15,944,762-17,090,017 SNHG29, ZNF624, 46 more genes
    nsv7059177inversion1nstd229human GRCh38 chr17: 15,493,473-18,338,296 , GRCh37.p13 chr17: 15,396,787-18,241,610 TOM1L2, PPIAP53, 107 more genes
    nsv6997737copy number variation1nstd229human GRCh38 chr17: 16,347,446-16,616,929 , GRCh37.p13 chr17: 16,250,760-16,520,243 SNORD49A, LOC105371554, 11 more genes
    nsv6996874copy number variation1nstd229human GRCh38 chr17: 16,439,706-16,440,203 , GRCh37.p13 chr17: 16,343,020-16,343,517 SNHG29, SNORD49B, 3 more genes
    nsv6995851copy number variation1nstd229human GRCh38 chr17: 16,261,589-17,283,740 , GRCh37.p13 chr17: 16,164,903-17,187,054 SRP68P1, SNORD49B, 42 more genes
    nsv6995108copy number variation1nstd229human GRCh38 chr17: 16,439,415-16,439,526 , GRCh37.p13 chr17: 16,342,729-16,342,840 SNHG29, SNORD49A, 2 more genes
    nsv6994792copy number variation1nstd229human GRCh38 chr17: 16,455,901-16,459,500 , GRCh37.p13 chr17: 16,359,215-16,362,814 SNHG29, LRRC75A
    nsv6993292copy number variation1nstd229human GRCh38 chr17: 16,424,735-16,451,294 , GRCh37.p13 chr17: 16,328,049-16,354,608 SNORD49A, SNORD65, 4 more genes
    nsv6988331copy number variation1nstd229human GRCh38 chr17: 16,462,619-16,462,777 , GRCh37.p13 chr17: 16,365,933-16,366,091 SNHG29, LRRC75A
    nsv6985891copy number variation1nstd229human GRCh38 chr17: 16,453,250-16,522,031 , GRCh37.p13 chr17: 16,356,564-16,425,345 SNHG29, LRRC75A
    nsv6979797copy number variation1nstd229human GRCh38 chr17: 16,368,854-16,586,406 , GRCh37.p13 chr17: 16,272,168-16,489,720 FTLP12, LOC105371554, 8 more genes
    nsv6637693copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,754,174-16,657,319 , GRCh38.p12 chr17: 15,850,860-16,754,005 SNORD65, RN7SL442P, 29 more genes
    nsv6637587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,293,557-16,421,075 , GRCh38.p12 chr17: 16,390,243-16,517,761 SNORD49A, SNORD65, 5 more genes
    nsv6637557copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,722,840-16,653,256 , GRCh38.p12 chr17: 15,819,526-16,749,942 RPLP1P11, SNORD49A, 31 more genes
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