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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv7050922inversion1nstd229human GRCh38 chr4: 81,449,891-81,449,938 , GRCh37.p13 chr4: 82,371,045-82,371,092 RASGEF1B
    nsv7049185inversion1nstd229human GRCh38 chr4: 77,808,799-83,184,403 , GRCh37.p13 chr4: 78,729,953-84,105,556 VAMP9P, HNRNPA3P13, 75 more genes
    nsv7039946inversion1nstd229human GRCh38 chr4: 81,128,223-81,477,725 , GRCh37.p13 chr4: 82,049,377-82,398,879 PRKG2-AS1, RNU5A-2P, 2 more genes
    nsv6757941copy number variation1nstd229human GRCh38 chr4: 81,363,532-81,455,117 , GRCh37.p13 chr4: 82,284,686-82,376,271 RASGEF1B
    nsv6757534copy number variation1nstd229human GRCh38 chr4: 81,350,452-81,747,755 , GRCh37.p13 chr4: 82,271,606-82,668,909 RASGEF1B, LOC105377306, 1 more genes
    nsv6748290copy number variation1nstd229human GRCh38 chr4: 81,451,497-81,457,534 , GRCh37.p13 chr4: 82,372,651-82,378,688 RASGEF1B
    nsv6747265copy number variation1nstd229human GRCh38 chr4: 81,445,417-81,445,470 , GRCh37.p13 chr4: 82,366,571-82,366,624 RASGEF1B
    nsv6741769copy number variation1nstd229human GRCh38 chr4: 81,423,795-81,426,806 , GRCh37.p13 chr4: 82,344,949-82,347,960 RASGEF1B
    nsv6636945copy number variation1nstd102humanUncertain significance GRCh37 chr4: 82,377,883-82,417,592 , GRCh38.p12 chr4: 81,456,729-81,496,438 RASGEF1B
    nsv6629989copy number variation1nstd224human GRCh37 chr4: 82,226,349-82,382,526 , GRCh38.p12 chr4: 81,305,195-81,461,372 RNU5A-2P, RASGEF1B
    nsv6565136inversion1nstd223human GRCh38 chr4: 74,413,523-83,001,891 , GRCh37.p13 chr4: 75,279,240-83,923,044 RNU6-615P, SHROOM3, 144 more genes
    nsv6389855copy number variation1nstd223human GRCh38 chr4: 81,435,676-82,210,038 , GRCh37.p13 chr4: 82,356,830-83,131,191 COX5BP1, NPM1P41, 5 more genes
    nsv6389655copy number variation1nstd223human GRCh38 chr4: 81,374,301-81,722,900 , GRCh37.p13 chr4: 82,295,455-82,644,054 LOC105377306, RASGEF1B
    nsv6314916copy number variation1nstd102humanPathogenic GRCh38 chr4: 67,833,055-82,716,065 , GRCh37.p13 chr4: 68,698,773-83,637,218 MICOS10P4, SULT1B1, 274 more genes
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 RPL6P13, SNORD144, 136 more genes
    nsv6313633copy number variation1nstd102humanUncertain significance GRCh37 chr4: 80,865,788-82,927,188 , GRCh38.p12 chr4: 79,944,634-82,006,035 RASGEF1B, BMP3, 16 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 LOC105377329, LOC107986294, 166 more genes
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