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Items: 1 to 20 of 34908

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137811delins1nstd102humanUncertain significance GRCh37 chrX: 153,135,874-153,135,931 , GRCh38 chrX: 153,870,419-153,870,476 L1CAM
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6137707copy number variation1nstd102humanPathogenic GRCh37 chr16: 29,565,626-30,221,925 , GRCh38.p12 chr16: 29,554,305-30,210,604 TAOK2, SLC7A5P1, 44 more genes
    nsv6137672copy number variation1nstd102humannot provided GRCh38 chr2: 124,348,648-129,410,245 , GRCh37.p13 chr2: 125,106,225-130,167,818 LOC105373603, MYO7B, 59 more genes
    nsv6131637insertion1nstd186human GRCh37 chr16: 31,313,771-31,313,792 , GRCh38.p12 chr16: 31,302,450-31,302,471 ITGAM
    nsv6131470insertion1nstd186human GRCh37 chr19: 41,849,848-41,849,872 , GRCh38.p12 chr19: 41,343,943-41,343,967 TGFB1
    nsv6131390insertion1nstd186human GRCh37 chr17: 48,140,446-48,140,448 , GRCh38.p12 chr17: 50,063,082-50,063,084 ITGA3
    nsv6131054insertion1nstd186human GRCh37 chr16: 30,511,055-30,511,105 , GRCh38.p12 chr16: 30,499,734-30,499,784 ITGAL
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6130429insertion1nstd186human GRCh37 chr20: 33,801,730-33,801,781 , GRCh38.p12 chr20: 35,213,927-35,213,978 PROCR, MMP24-AS1-EDEM2
    nsv6129074copy number variation1nstd186human GRCh37 chr19: 566,126-569,393 , GRCh38.p12 chr19: 566,126-569,393 BSG-AS1, BSG
    nsv6128950copy number variation1nstd186human GRCh37 chr19: 43,399,886-43,408,213 , GRCh38.p12 chr19: 42,895,734-42,904,061 PSG6
    nsv6128577copy number variation1nstd186human GRCh37 chr19: 43,682,254-43,701,331 , GRCh38.p12 chr19: 43,178,102-43,197,179 PSG4, PSG5, 1 more genes
    nsv6127905copy number variation1nstd186human GRCh37 chr19: 43,645,584-43,745,072 , GRCh38.p12 chr19: 43,141,432-43,240,920 , CEACAMP10, 4 more genes
    nsv6127247copy number variation1nstd186human GRCh37 chr19: 43,507,854-43,753,339 , GRCh38.p12 chr19: 43,003,702-43,249,187 , LOC284344, 8 more genes
    nsv6126994copy number variation1nstd186human GRCh37 chr19: 43,293,170-43,547,819 , GRCh38.p12 chr19: 42,789,018-43,043,667 CEACAMP7, CEACAMP8, 6 more genes
    nsv6126127copy number variation1nstd186human GRCh37 chr21: 46,338,850-46,338,935 , GRCh38.p12 chr21: 44,918,935-44,919,020 ITGB2
    nsv6126101copy number variation1nstd186human GRCh37 chr19: 43,700,936-43,764,804 , GRCh38.p12 chr19: 43,196,784-43,260,652 CEACAMP10, PSG4, 2 more genes
    nsv6125854copy number variation1nstd186human GRCh37 chr19: 43,363,237-43,387,115 , GRCh38.p12 chr19: 42,859,085-42,882,963 PSG1
    nsv6125428copy number variation1nstd186human GRCh37 chr19: 43,612,483-43,677,266 , GRCh38.p12 chr19: 43,108,331-43,173,114 , PSG5
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