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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137216copy number variation1nstd102humanPathogenic GRCh37 chr17: 30,572,862-35,843,988 , GRCh38.p12 chr17: 32,245,843-36,446,544 PSMD11, C17orf50, 117 more genes
    nsv7095147copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,475,283-34,079,869 , GRCh38.p12 chr17: 35,148,264-35,752,850 SLC35G3, AP2B1, 26 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6996845copy number variation1nstd229human GRCh38 chr17: 35,240,913-35,267,991 , GRCh37.p13 chr17: 33,567,932-33,595,010 LOC105371932, SLFN5
    nsv6995184copy number variation1nstd229human GRCh38 chr17: 35,242,424-35,242,470 , GRCh37.p13 chr17: 33,569,443-33,569,489 SLFN5, LOC105371932
    nsv6994838copy number variation1nstd229human GRCh38 chr17: 35,170,807-35,536,994 , GRCh37.p13 chr17: 33,497,826-33,864,013 SLFN5, SPICP2, 15 more genes
    nsv6994272copy number variation1nstd229human GRCh38 chr17: 35,248,248-35,252,860 , GRCh37.p13 chr17: 33,575,267-33,579,879 SLFN5
    nsv6993920copy number variation1nstd229human GRCh38 chr17: 35,252,151-35,260,482 , GRCh37.p13 chr17: 33,579,170-33,587,501 SLFN5
    nsv6993239copy number variation1nstd229human GRCh38 chr17: 35,167,502-35,536,993 , GRCh37.p13 chr17: 33,494,521-33,864,012 LOC105371932, SLC35G3, 15 more genes
    nsv6989496copy number variation1nstd229human GRCh38 chr17: 35,249,304-35,259,009 , GRCh37.p13 chr17: 33,576,323-33,586,028 SLFN5
    nsv6984332copy number variation1nstd229human GRCh38 chr17: 35,244,824-35,250,407 , GRCh37.p13 chr17: 33,571,843-33,577,426 LOC105371932, SLFN5
    nsv6982202copy number variation1nstd229human GRCh38 chr17: 34,998,758-35,727,529 , GRCh37.p13 chr17: 33,325,777-34,034,851 SLFN11, LOC105371932, 32 more genes
    nsv6594697inversion1nstd223human GRCh38 chr17: 35,261,675-35,262,379 , GRCh37.p13 chr17: 33,588,694-33,589,398 SLFN5
    nsv6515133copy number variation1nstd223human GRCh38 chr17: 35,244,830-35,250,397 , GRCh37.p13 chr17: 33,571,849-33,577,416 LOC105371932, SLFN5
    nsv6500991copy number variation1nstd223human GRCh38 chr17: 35,250,446-35,254,738 , GRCh37.p13 chr17: 33,577,465-33,581,757 SLFN5
    nsv6499851copy number variation1nstd223human GRCh38 chr17: 34,998,758-35,727,531 , GRCh37.p13 chr17: 33,325,777-34,034,851 FNDC8, LOC101060119, 32 more genes
    nsv6497486copy number variation1nstd223human GRCh38 chr17: 34,547,647-35,364,191 , GRCh37.p13 chr17: 32,874,666-33,691,210 LOC105371742, ZNF830, 19 more genes
    nsv6133353copy number variation1nstd213human GRCh37 chr17: 33,210,000-34,670,001 , GRCh38.p12 chr17: 34,882,981-35,919,248 AP2B1, E2F3P1, 48 more genes
    nsv6133304copy number variation1nstd213human GRCh37 chr17: 33,600,000-33,760,001 , GRCh38.p12 chr17: 35,272,981-35,432,982 SLFN12, SLFN11, 5 more genes
    nsv6133243copy number variation1nstd213human GRCh37 chr17: 33,420,000-33,600,001 , GRCh38.p12 chr17: 35,092,981-35,272,982 RAD51D, NLE1, 7 more genes
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