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Items: 1 to 20 of 983

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145691copy number variation1nstd232human GRCh37.p13 chr15: 30,668,102-30,668,187 , GRCh38.p12 chr15: 30,375,899-30,375,984 , GRCh38.p12 chr15|NT_187660.1: 2,660,803-2,660,859 , GRCh38.p12 chr15|NW_011332701.1: 2,548,319-2,548,375 CHRFAM7A
    nsv7144558insertion1nstd232human GRCh37.p13 chr15: 31,715,336-31,715,336 , GRCh38.p12 chr15: 31,423,133-31,423,133 , GRCh38.p12 chr15|NT_187660.1: 3,708,970-3,708,970 , GRCh38.p12 chr15|NW_011332701.1: 3,596,518-3,596,518 KLF13
    nsv7142844insertion1nstd232human GRCh37.p13 chr15: 29,853,208-29,853,208 , GRCh38.p12 chr15: 29,561,004-29,561,004 , GRCh38.p12 chr15|NT_187660.1: 1,838,320-1,838,320 , GRCh38.p12 chr15|NW_011332701.1: 1,725,836-1,725,836 ENTREP2
    nsv7142712copy number variation1nstd232human GRCh37.p13 chr15: 29,880,726-29,880,792 , GRCh38.p12 chr15: 29,588,522-29,588,588 , GRCh38.p12 chr15|NT_187660.1: 1,872,684-1,872,748 , GRCh38.p12 chr15|NW_011332701.1: 1,760,200-1,760,264 0
    nsv7142284insertion1nstd232human GRCh37.p13 chr15: 31,715,379-31,715,379 , GRCh38.p12 chr15: 31,423,176-31,423,176 , GRCh38.p12 chr15|NT_187660.1: 3,709,013-3,709,013 , GRCh38.p12 chr15|NW_011332701.1: 3,596,561-3,596,561 KLF13
    nsv7138655copy number variation1nstd232human GRCh37.p13 chr15: 32,358,109-32,358,184 , GRCh38.p12 chr15: 32,065,906-32,065,981 , GRCh38.p12 chr15|NT_187660.1: 4,351,038-4,351,113 , GRCh38.p12 chr15|NW_011332701.1: 4,238,586-4,238,661 CHRNA7
    nsv7137205copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,073,735-32,446,830 , GRCh38.p12 chr15: 30,781,532-32,154,629 , GRCh38.p12 chr15|NW_011332701.1: 2,954,785-4,327,333 , GRCh38.p12 chr15|NT_187660.1: 3,067,237-4,439,785 UBE2CP4, LOC107984779, 21 more genes
    nsv7136957copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,538,169-28,566,507 , GRCh38.p12 chr15: 28,293,023-28,321,361 , GRCh38.p12 chr15|NT_187660.1: 540,248-568,585 , GRCh38.p12 chr15|NW_011332701.1: 426,462-454,799 HERC2, RPL41P2
    nsv7136954copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,196,075-31,233,768 , GRCh38.p12 chr15|NT_187660.1: 3,189,604-3,227,294 , GRCh38.p12 chr15: 30,903,872-30,941,565 , GRCh38.p12 chr15|NW_011332701.1: 3,077,152-3,114,842 MTMR10, FAN1
    nsv7094527copy number variation2nstd102humanUncertain significance GRCh37 chr15: 29,560,995-29,561,909 , GRCh38.p12 chr15|NW_011332701.1: 1,431,858-1,432,772 , GRCh38.p12 chr15|NT_187660.1: 1,544,342-1,545,256 , GRCh38.p12 chr15: 29,268,791-29,269,705 ENTREP2, NSMCE3
    nsv7094526copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 28,544,548-28,544,662 , GRCh38.p12 chr15: 28,299,402-28,299,516 , GRCh38.p12 chr15|NT_187660.1: 546,626-546,740 , GRCh38.p12 chr15|NW_011332701.1: 432,840-432,954 HERC2
    nsv7094525copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,235,702-28,277,329 , GRCh38.p12 chr15|NT_187660.1: 124,825-166,482 , GRCh38.p12 chr15|NW_011332701.1: 124,825-166,482 , GRCh38.p12 chr15: 27,990,556-28,032,183 OCA2
    nsv7094465copy number variation1nstd102humanUncertain significance GRCh37 chr15: 31,196,867-34,112,028 , GRCh38.p12 chr15: 30,904,664-33,819,827 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 , GRCh38.p12 chr15|NW_011332701.1: 3,077,944-4,998,962 RNU6-18P, CHRNA7, 72 more genes
    nsv7094463copy number variation2nstd102humanPathogenic GRCh37 chr15: 28,171,253-28,277,329 , GRCh38.p12 chr15|NW_011332701.1: 60,394-166,482 , GRCh38.p12 chr15: 27,926,107-28,032,183 , GRCh38.p12 chr15|NT_187660.1: 60,394-166,482 OCA2
    nsv7094363copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,326,774-28,327,020 , GRCh38.p12 chr15: 28,081,628-28,081,874 , GRCh38.p12 chr15|NT_187660.1: 215,928-216,174 , GRCh38.p12 chr15|NW_011332701.1: 215,928-216,174 OCA2
    nsv7094362copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,267,627-28,391,510 , GRCh38.p12 chr15: 28,022,481-28,146,364 , GRCh38.p12 chr15|NT_187660.1: 156,780-279,806 , GRCh38.p12 chr15|NW_011332701.1: 156,780-279,806 OCA2, HERC2
    nsv7094361copy number variation1nstd102humanUncertain significance GRCh37 chr15: 28,259,902-28,261,352 , GRCh38.p12 chr15: 28,014,756-28,016,206 , GRCh38.p12 chr15|NT_187660.1: 149,056-150,506 , GRCh38.p12 chr15|NW_011332701.1: 149,056-150,506 OCA2
    nsv7094360copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,234,727-28,234,832 , GRCh38.p12 chr15: 27,989,581-27,989,686 , GRCh38.p12 chr15|NW_011332701.1: 123,850-123,955 , GRCh38.p12 chr15|NT_187660.1: 123,850-123,955 OCA2
    nsv7094281copy number variation1nstd102humanUncertain significance GRCh37 chr15: 32,393,486-34,030,811 , GRCh38.p12 chr15: 32,101,283-33,738,610 , GRCh38.p12 chr15|NT_187660.1: 2,721,316-5,161,414 ARHGAP11B, TMCO5B, 72 more genes
    nsv7094279copy number variation1nstd102humanPathogenic GRCh37 chr15: 28,211,816-28,211,988 , GRCh38.p12 chr15|NT_187660.1: 100,949-101,121 , GRCh38.p12 chr15: 27,966,670-27,966,842 , GRCh38.p12 chr15|NW_011332701.1: 100,949-101,121 OCA2
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