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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057970inversion1nstd229human GRCh38 chr5: 39,369,727-42,623,585 , GRCh37.p13 chr5: 39,369,829-42,623,687 LINC02996, DAB2, 36 more genes
    nsv7057876inversion1nstd229human GRCh38 chr5: 40,785,368-40,874,865 , GRCh37.p13 chr5: 40,785,470-40,874,967 RPL37, SNORD72, 2 more genes
    nsv7053304inversion1nstd229human GRCh38 chr5: 40,805,318-40,878,894 , GRCh37.p13 chr5: 40,805,420-40,878,996 CARD6, SNORD72, 1 more genes
    nsv7041157inversion1nstd229human GRCh38 chr5: 40,200,630-42,327,400 , GRCh37.p13 chr5: 40,200,732-42,327,502 RNU7-161P, LINC02996, 26 more genes
    nsv6777504copy number variation1nstd229human GRCh38 chr5: 40,715,401-40,932,800 , GRCh37.p13 chr5: 40,715,503-40,932,902 RNU7-161P, RPL37, 6 more genes
    nsv6774610copy number variation1nstd229human GRCh38 chr5: 40,819,073-40,830,372 , GRCh37.p13 chr5: 40,819,175-40,830,474 RPL37
    nsv6774543copy number variation1nstd229human GRCh38 chr5: 40,828,451-40,828,516 , GRCh37.p13 chr5: 40,828,553-40,828,618 RPL37
    nsv6769814copy number variation1nstd229human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 RNU7-161P, OXCT1, 35 more genes
    nsv6768943copy number variation1nstd229human GRCh38 chr5: 40,583,586-41,276,040 , GRCh37.p13 chr5: 40,583,688-41,276,142 TTC33, RPL37, 10 more genes
    nsv6768573copy number variation1nstd229human GRCh38 chr5: 40,817,001-40,824,300 , GRCh37.p13 chr5: 40,817,103-40,824,402 RPL37
    nsv6763566copy number variation1nstd229human GRCh38 chr5: 40,821,884-40,826,006 , GRCh37.p13 chr5: 40,821,986-40,826,108 RPL37
    nsv6763460copy number variation1nstd229human GRCh38 chr5: 39,215,959-40,973,214 , GRCh37.p13 chr5: 39,216,061-40,973,316 PRKAA1, PTGER4, 18 more genes
    nsv6761804copy number variation1nstd229human GRCh38 chr5: 40,833,724-40,833,785 , GRCh37.p13 chr5: 40,833,826-40,833,887 RPL37
    nsv6761216copy number variation1nstd229human GRCh38 chr5: 40,785,401-40,859,200 , GRCh37.p13 chr5: 40,785,503-40,859,302 RPL37, CARD6, 2 more genes
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6388671copy number variation1nstd223human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 SERBP1P6, TCP1P2, 35 more genes
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6297521copy number variation1nstd186human GRCh37 chr5: 40,833,097-40,833,189 , GRCh38.p12 chr5: 40,832,995-40,833,087 RPL37, SNORD72
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