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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094922copy number variation1nstd102humanUncertain significance GRCh37 chr17: 77,752,035-77,752,246 , GRCh38.p12 chr17: 79,778,236-79,778,447 CBX2
    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
    nsv7068289inversion1nstd229human GRCh38 chr17: 79,670,537-79,779,397 , GRCh37.p13 chr17: 77,644,399-77,753,196 , GRCh37.p13 chr17|NW_003871089.1: 254,543-363,403 CBX2, LINC02078, 2 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
    nsv6989995copy number variation1nstd229human GRCh38 chr17: 79,761,461-79,781,811 , GRCh37.p13 chr17: 77,735,260-77,755,610 , GRCh37.p13 chr17|NW_003871089.1: 345,467-365,817 CBX2
    nsv6986269copy number variation1nstd229human GRCh38 chr17: 79,779,499-79,779,618 , GRCh37.p13 chr17|NW_003871089.1: 363,505-363,624 , GRCh37.p13 chr17: 77,753,298-77,753,417 CBX2
    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
    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
    nsv6525566copy number variation1nstd223human GRCh38 chr17: 79,774,734-79,775,380 , GRCh37.p13 chr17: 77,748,533-77,749,179 , GRCh37.p13 chr17|NW_003871089.1: 358,740-359,386 CBX2
    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
    nsv6259104mobile element insertion1nstd215human GRCh38 chr17: 79,775,914-79,775,914 , GRCh37.p13 chr17|NW_003871089.1: 359,920-359,920 , GRCh37.p13 chr17: 77,749,713-77,749,713 CBX2
    nsv6115531mobile element insertion1nstd186human GRCh37 chr17: 77,749,713-77,749,764 , GRCh38.p12 chr17: 79,775,914-79,775,965 CBX2
    nsv6083272insertion1nstd212human GRCh38 chr17: 79,775,907-79,775,907 , GRCh37.p13 chr17|NW_003871089.1: 359,913-359,913 , GRCh37.p13 chr17: 77,749,706-77,749,706 CBX2
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