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Items: 1 to 20 of 153

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140140copy number variation1nstd232human GRCh37.p13 chr17: 12,898,201-12,898,278 , GRCh38.p12 chr17: 12,994,884-12,994,961 ELAC2
    nsv7139546copy number variation1nstd232human GRCh37.p13 chr17: 12,905,676-12,905,756 , GRCh38.p12 chr17: 13,002,359-13,002,439 ELAC2
    nsv7093605insertion1nstd102humanUncertain significance GRCh37 chr17: 12,920,236-12,920,236 , GRCh38 chr17: 13,016,919-13,016,919 ELAC2
    nsv6997372copy number variation1nstd229human GRCh38 chr17: 13,003,328-13,010,875 , GRCh37.p13 chr17: 12,906,645-12,914,192 ELAC2
    nsv6995769copy number variation1nstd229human GRCh38 chr17: 12,884,733-13,059,494 , GRCh37.p13 chr17: 12,788,050-12,962,811 ARHGAP44, MIR1269B, 1 more genes
    nsv6988010copy number variation1nstd229human GRCh38 chr17: 12,938,583-13,070,068 , GRCh37.p13 chr17: 12,841,900-12,973,385 ELAC2, ARHGAP44
    nsv6979351copy number variation1nstd229human GRCh38 chr17: 12,688,917-15,327,390 , GRCh37.p13 chr17: 12,592,234-15,230,707 PMP22, COX10-DT, 32 more genes
    nsv6507862copy number variation1nstd223human GRCh38 chr17: 13,006,859-13,007,615 , GRCh37.p13 chr17: 12,910,176-12,910,932 ELAC2
    nsv6498918copy number variation1nstd223human GRCh38 chr17: 12,857,541-13,010,336 , GRCh37.p13 chr17: 12,760,858-12,913,653 ARHGAP44, ELAC2, 1 more genes
    nsv6315277copy number variation1nstd102humanPathogenic GRCh38 chr17: 11,915,997-17,892,664 , GRCh37.p13 chr17: 11,819,314-17,795,978 LINC02087, USP32P1, 135 more genes
    nsv6310121copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,920,159-12,920,458 , GRCh38.p12 chr17: 13,016,842-13,017,141 ELAC2
    nsv6310055copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr17: 12,896,135-12,921,264 , GRCh38.p12 chr17: 12,992,818-13,017,947 ELAC2
    nsv6310045copy number variation1nstd102humanUncertain significance GRCh37 chr17: 12,896,683-12,896,998 , GRCh38 chr17: 12,993,366-12,993,681 ELAC2
    nsv6309964copy number variation1nstd102humanUncertain significance GRCh37 chr17: 12,896,135-12,909,316 , GRCh38.p12 chr17: 12,992,818-13,005,999 ELAC2
    nsv6291529copy number variation1nstd102humannot provided GRCh37 chr17: 12,524,223-16,047,567 , GRCh38.p12 chr17: 12,620,906-16,144,253 LOC107984976, SPECC1P1, 64 more genes
    nsv6285306insertion1nstd214human GRCh38 chr17: 12,992,883-12,992,883 , GRCh37.p13 chr17: 12,896,200-12,896,200 ELAC2
    nsv6147068sequence alteration1nstd206human GRCh38 chr17: 12,914,601-13,028,662 , GRCh37.p13 chr17: 12,817,918-12,931,979 ARHGAP44, ELAC2, 1 more genes
    nsv6133324copy number variation1nstd213human GRCh37 chr17: 9,930,000-12,980,001 , GRCh38.p12 chr17: 10,026,683-13,076,684 DNAH9, MYH1, 36 more genes
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5564311copy number variation1nstd102humanUncertain significance GRCh37 chr17: 12,896,201-12,896,263 , GRCh38.p12 chr17: 12,992,884-12,992,946 ELAC2
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