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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 76,851,749-78,367,298 , GRCh38.p12 chr17: 78,855,667-80,393,498 RNF213-AS1, EIF4A3, 25 more genes
    nsv7072983inversion1nstd229human GRCh38 chr17: 79,606,852-81,315,890 , GRCh37.p13 chr17: 77,766,017-79,289,690 MIR4739, MIR4730, 44 more genes
    nsv7071296inversion1nstd229human GRCh38 chr17: 79,045,634-82,531,412 , GRCh37.p13 chr17: 77,041,716-80,489,288 , ENPP7, 111 more genes
    nsv7067212inversion1nstd229human GRCh38 chr17: 79,320,851-81,127,081 , GRCh37.p13 chr17: 77,316,933-79,100,881 RPL32P31, RPTOR, 35 more genes
    nsv7065384inversion1nstd229human GRCh38 chr17: 79,173,003-81,030,493 , GRCh37.p13 chr17: 77,169,085-79,004,293 GAA, ENPP7, 30 more genes
    nsv7061803inversion1nstd229human GRCh38 chr17: 79,169,515-81,031,248 , GRCh37.p13 chr17: 77,165,597-79,005,048 CBX4, SLC26A11, 30 more genes
    nsv6993667copy number variation1nstd229human GRCh38 chr17: 78,709,580-81,173,842 , GRCh37.p13 chr17: 76,705,662-79,147,642 C1QTNF1-AS1, NPTX1, 47 more genes
    nsv6985053copy number variation1nstd229human GRCh38 chr17: 79,723,795-79,950,306 , GRCh37.p13 chr17: 77,766,017-77,924,105 CBX4, LINC01977, 6 more genes
    nsv6985046copy number variation1nstd229human GRCh38 chr17: 79,831,150-79,831,231 , GRCh37.p13 chr17: 77,804,949-77,805,030 CBX4
    nsv6982764copy number variation1nstd229human GRCh38 chr17: 79,598,509-79,919,141 , GRCh37.p13 chr17|NW_003871089.1: 182,515-376,223 CBX4, MIR4739, 8 more genes
    nsv6979172copy number variation1nstd229human GRCh38 chr17: 79,761,601-79,834,800 , GRCh37.p13 chr17: 77,766,017-77,808,599 CBX4, LINC01977, 2 more genes
    nsv6535248copy number variation1nstd223human GRCh38 chr17: 79,837,486-79,837,727 , GRCh37.p13 chr17: 77,811,285-77,811,526 CBX4
    nsv6315182copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,481,509-81,043,199 , GRCh38.p12 chr17: 75,485,428-83,085,323 DUS1L, PVALEF, 252 more genes
    nsv6314160copy number variation1nstd102humanUncertain significance GRCh37 chr17: 77,641,336-79,465,235 , GRCh38.p12 chr17: 79,667,474-81,498,209 BAIAP2-DT, SLC38A10, 49 more genes
    nsv6285753insertion1nstd214human GRCh38 chr17: 79,831,159-79,831,159 , GRCh37.p13 chr17: 77,804,958-77,804,958 CBX4
    nsv6094278insertion1nstd212human GRCh38 chr17: 79,831,218-79,831,218 , GRCh37.p13 chr17: 77,805,017-77,805,017 CBX4
    nsv6026648copy number variation1nstd212human GRCh38 chr17: 79,831,182-79,831,235 , GRCh37.p13 chr17: 77,804,981-77,805,034 CBX4
    nsv5349721translocation1nstd200human GRCh38 chr17: 79,831,537-79,831,537 , GRCh38 chr17: 79,831,589-79,831,589 , GRCh37.p13 chr17: 77,805,336-77,805,336 , GRCh37.p13 chr17: 77,805,388-77,805,388 CBX4
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4531945copy number variation1nstd166human GRCh37.p13 chr17: 77,804,873-77,804,977 , GRCh38.p12 chr17: 79,831,074-79,831,178 CBX4
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