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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5919512copy number variation1nstd209human GRCh38 chr7: 26,509,679-33,120,288 , GRCh37.p13 chr7: 26,549,298-33,159,900 , CPVL-AS1, 126 more genes
    nsv5914132copy number variation1nstd209human GRCh38 chr7: 26,936,027-36,716,695 , GRCh37.p13 chr7: 26,975,646-36,756,300 , HOXA7, 162 more genes
    nsv5565769copy number variation1nstd207human GRCh38 chr7: 30,495,983-30,496,308 , GRCh37.p13 chr7: 30,535,599-30,535,924 GGCT
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5383166mobile element deletion2nstd186human GRCh37 chr7: 30,535,601-30,535,911 , GRCh38.p12 chr7: 30,495,985-30,496,295 GGCT
    nsv5310752copy number variation1nstd204human GRCh38.p13 chr7: 30,478,183-30,502,363 , GRCh37.p13 chr7: 30,517,799-30,541,979 NOD1, GGCT
    nsv5222071copy number variation1nstd204human GRCh38.p13 chr7: 30,477,572-30,501,695 , GRCh37.p13 chr7: 30,517,188-30,541,311 NOD1, GGCT
    nsv5218818mobile element deletion1nstd204human GRCh38.p13 chr7: 30,495,985-30,496,295 , GRCh37.p13 chr7: 30,535,601-30,535,911 GGCT
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4953550copy number variation1nstd200human GRCh38 chr7: 30,478,193-30,502,356 , GRCh37.p13 chr7: 30,517,809-30,541,972 NOD1, GGCT
    nsv4888271mobile element deletion1nstd200human GRCh38 chr7: 30,495,985-30,496,295 , GRCh37.p13 chr7: 30,535,601-30,535,911 GGCT
    nsv4882608inversion1nstd200human GRCh37 chr7: 6,326,174-37,121,976 , GRCh38.p12 chr7: 6,286,543-37,082,371 , HOXA13, 435 more genes
    nsv4828850copy number variation1nstd200human GRCh37 chr7: 30,517,809-30,541,972 , GRCh38.p12 chr7: 30,478,193-30,502,356 NOD1, GGCT
    nsv4787195mobile element deletion1nstd200human GRCh37 chr7: 30,535,601-30,535,911 , GRCh38.p12 chr7: 30,495,985-30,496,295 GGCT
    nsv4740778copy number variation1nstd199human GRCh37 chr7: 30,535,590-30,535,918 , GRCh38.p12 chr7: 30,495,974-30,496,302 GGCT
    nsv4729079copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 29,758,030-31,318,843 , GRCh38.p12 chr7: 29,718,414-31,279,229 ADCYAP1R1, AQP1, 33 more genes
    nsv4713739copy number variation3nstd195human GRCh37 chr7: 30,535,583-30,535,584 , GRCh38.p12 chr7: 30,495,967-30,495,968 GGCT
    nsv4676067copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,502,942-30,888,964 , GRCh38.p12 chr7: 30,463,326-30,849,348 GARS1-DT, NOD1, 9 more genes
    nsv4675863copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 28,487,175-32,037,495 , GRCh38.p12 chr7: 28,447,557-31,997,883 ADCYAP1R1, AQP1, 55 more genes
    nsv4675226copy number variation1nstd102humanUncertain significance GRCh37 chr7: 30,463,886-30,674,061 , GRCh38.p12 chr7: 30,424,270-30,634,445 LOC100287825, GARS1, 3 more genes
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