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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148249copy number variation1nstd102humanPathogenic GRCh38 chr6: 113,857,248-130,442,177 , GRCh37.p13 chr6: 114,178,427-130,763,322 TRDN-AS1, LOC100420743, 179 more genes
    nsv7137202copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 112,713,854-124,105,184 , GRCh38.p12 chr6: 112,392,652-123,784,039 COL10A1, FABP7, 129 more genes
    nsv7097176copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,441,236-119,252,888 , GRCh38.p12 chr6: 116,120,073-118,931,723 RN7SKP18, COL10A1, 49 more genes
    nsv7057090inversion1nstd229human GRCh38 chr6: 112,695,234-116,359,280 , GRCh37.p13 chr6: 113,016,436-116,680,443 MARCKS, TSPYL1, 42 more genes
    nsv7051708inversion1nstd229human GRCh38 chr6: 115,507,946-121,145,291 , GRCh37.p13 chr6: 115,829,110-121,466,437 COL10A1, KRT18P22, 67 more genes
    nsv7043912inversion1nstd229human GRCh38 chr6: 113,606,593-119,197,751 , GRCh37.p13 chr6: 113,927,795-119,518,916 TPI1P3, CALHM5, 73 more genes
    nsv6817684copy number variation1nstd229human GRCh38 chr6: 116,142,876-116,329,891 , GRCh37.p13 chr6: 116,464,039-116,651,054 TSPYL1, RPS5P1, 5 more genes
    nsv6811726copy number variation1nstd229human GRCh38 chr6: 116,234,289-116,248,999 , GRCh37.p13 chr6: 116,555,452-116,570,162 NT5DC1, TSPYL4
    nsv6810572copy number variation1nstd229human GRCh38 chr6: 116,018,631-116,666,979 , GRCh37.p13 chr6: 116,339,794-116,988,142 FRK, TPI1P3, 18 more genes
    nsv6808061copy number variation1nstd229human GRCh38 chr6: 116,066,906-116,438,245 , GRCh37.p13 chr6: 116,388,069-116,759,408 RPS5P1, NT5DC1, 8 more genes
    nsv6801670copy number variation1nstd229human GRCh38 chr6: 115,990,464-116,275,885 , GRCh37.p13 chr6: 116,311,627-116,597,048 DSE, NIP7P3, 8 more genes
    nsv6798127copy number variation1nstd229human GRCh38 chr6: 116,114,423-116,353,577 , GRCh37.p13 chr6: 116,435,586-116,674,740 NT5DC1, DSE, 6 more genes
    nsv6630707copy number variation1nstd224human GRCh37 chr6: 116,406,736-116,650,558 , GRCh38.p12 chr6: 116,085,573-116,329,395 COL10A1, FRK, 7 more genes
    nsv6612342copy number variation1nstd223human GRCh38 chr6: 116,243,301-116,250,300 , GRCh37.p13 chr6: 116,564,464-116,571,463 TSPYL4, NT5DC1
    nsv6606808copy number variation1nstd223human GRCh38 chr6: 111,642,175-118,933,374 , GRCh37.p13 chr6: 111,963,378-119,254,539 COL10A1, LOC105377952, 106 more genes
    nsv6603085copy number variation1nstd223human GRCh38 chr6: 116,156,659-116,257,030 , GRCh37.p13 chr6: 116,477,822-116,578,193 COL10A1, TSPYL4, 4 more genes
    nsv6315321copy number variation1nstd102humanPathogenic GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791 SLC18B1, ARHGAP18, 223 more genes
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv6313666copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,212,698-119,482,708 , GRCh38.p12 chr6: 115,891,534-119,161,543 FAM184A, LOC107986523, 53 more genes
    nsv6291305copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,480,702-116,577,174 , GRCh38.p12 chr6: 116,159,539-116,256,011 TSPYL4, DSE, 2 more genes
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