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Items: 1 to 20 of 207

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097139copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-39,364,566 , GRCh38.p12 chr5: 33,944,648-39,364,464 RNU7-75P, UGT3A1, 77 more genes
    nsv7052596inversion1nstd229human GRCh38 chr5: 33,502,543-34,969,892 , GRCh37.p13 chr5: 33,502,648-34,969,997 TTC23L, DNAJC21, 22 more genes
    nsv7039407inversion1nstd229human GRCh38 chr5: 32,373,124-34,861,255 , GRCh37.p13 chr5: 32,373,230-34,861,360 TTC23L, LOC105374715, 31 more genes
    nsv6763595copy number variation1nstd229human GRCh38 chr5: 33,944,271-34,753,712 , GRCh37.p13 chr5: 33,944,376-34,753,817 RAI14-DT, C1QTNF3, 10 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
    nsv6572148inversion1nstd223human GRCh38 chr5: 33,560,391-36,411,977 , GRCh37.p13 chr5: 33,560,496-36,412,079 C1QTNF3, RAI14-DT, 36 more genes
    nsv6389179copy number variation1nstd223human GRCh38 chr5: 34,174,847-34,175,152 , GRCh37.p13 chr5: 34,174,952-34,175,257 C1QTNF3, GUSBP18
    nsv6387606copy number variation1nstd223human GRCh38 chr5: 34,175,325-34,485,599 , GRCh37.p13 chr5: 34,175,430-34,485,704 LOC646652, LOC105374719, 3 more genes
    nsv6383640copy number variation1nstd223human GRCh38 chr5: 34,175,903-34,176,462 , GRCh37.p13 chr5: 34,176,008-34,176,567 GUSBP18, C1QTNF3
    nsv6380333copy number variation1nstd223human GRCh38 chr5: 33,944,257-34,753,777 , GRCh37.p13 chr5: 33,944,362-34,753,882 GUSBP18, RAI14-DT, 10 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
    nsv6312292copy number variation1nstd102humanUncertain significance GRCh37 chr5: 34,007,858-34,935,958 , GRCh38.p12 chr5: 34,007,753-34,935,853 RAI14-DT, C1QTNF3, 14 more genes
    nsv6312196copy number variation1nstd102humanUncertain significance GRCh37 chr5: 33,944,753-35,089,722 , GRCh38.p12 chr5: 33,944,648-35,089,620 LOC100132524, AGXT2, 18 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
    nsv6141195copy number variation1nstd206human GRCh38 chr5: 34,174,872-34,175,177 , GRCh37.p13 chr5: 34,174,977-34,175,282 C1QTNF3, GUSBP18
    nsv6136111copy number variation1nstd213human GRCh37 chr5: 33,880,000-34,230,001 , GRCh38.p12 chr5: 33,879,895-34,229,896 SLC45A2, C1QTNF3, 8 more genes
    nsv6135406copy number variation1nstd213human GRCh37 chr5: 31,280,000-36,080,001 , GRCh38.p12 chr5: 31,279,893-36,079,899 IL7R, NPR3, 64 more genes
    nsv6135175copy number variation1nstd213human GRCh37 chr5: 29,210,000-46,400,001 , GRCh38.p12 chr5: 29,209,893-46,399,899 CDH6, HMGCS1, 210 more genes
    nsv5999454copy number variation1nstd212human GRCh38 chr5: 34,174,872-34,175,177 , GRCh37.p13 chr5: 34,174,977-34,175,282 C1QTNF3, GUSBP18
    nsv5898914copy number variation1nstd209human GRCh38 chr5: 34,174,872-34,175,176 , GRCh37.p13 chr5: 34,174,977-34,175,281 GUSBP18, C1QTNF3
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