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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976753inversion1nstd209human GRCh38 chr15: 77,155,274-77,261,494 , GRCh37.p13 chr15: 77,447,616-77,553,836 PEAK1, LINC00597, 1 more genes
    nsv5945672copy number variation1nstd209human GRCh38 chr15: 77,203,964-77,255,515 , GRCh37.p13 chr15: 77,496,306-77,547,857 LINC00597, PEAK1, 1 more genes
    nsv5945017copy number variation1nstd209human GRCh38 chr15: 77,209,292-77,282,294 , GRCh37.p13 chr15: 77,501,634-77,574,636 PEAK1, LINC00597, 1 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5037756inversion1nstd200human GRCh38 chr15: 75,735,812-77,868,882 , GRCh37.p13 chr15: 76,028,153-78,161,224 TRK-CTT16-1, SCAPER, 34 more genes
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4424799copy number variation1nstd174human GRCh37 chr15: 77,497,903-77,631,698 , GRCh38.p12 chr15: 77,205,561-77,339,356 LOC646853, PEAK1, 2 more genes
    nsv4382512copy number variation2nstd173human GRCh37 chr15: 77,506,427-77,576,602 , GRCh38.p12 chr15: 77,214,085-77,284,260 PEAK1, LINC00597, 1 more genes
    nsv4251531copy number variation1nstd166human GRCh37.p13 chr15: 77,517,494-77,522,626 , GRCh38.p12 chr15: 77,225,152-77,230,284 LINC00597, PEAK1
    nsv4247227copy number variation1nstd166human GRCh37.p13 chr15: 77,501,634-77,574,637 , GRCh38.p12 chr15: 77,209,292-77,282,295 LINC00597, PEAK1, 1 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
    nsv3915187copy number variation1nstd102humanPathogenic NCBI36 chr15: 70,234,344-100,278,724 , GRCh37 chr15: 72,447,290-102,461,201 , GRCh38 chr15: 72,154,949-101,920,998 LOC102724117, TMEM266, 618 more genes
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