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Items: 1 to 20 of 7896

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131509insertion1nstd186human GRCh37 chr17: 36,628,620-36,628,670 , GRCh38.p12 chr17: 38,472,379-38,472,429 , GRCh38.p12 chr17|NT_187614.1: 2,507,686-2,507,736 ARHGAP23
    nsv6131027insertion1nstd186human GRCh37 chr17: 35,197,146-35,197,179 , GRCh38.p12 chr17|NT_187614.1: 1,076,211-1,076,244 , GRCh38.p12 chr17: 36,839,877-36,839,910 0
    nsv6130995insertion1nstd186human GRCh37 chr17: 36,090,006-36,090,008 , GRCh38.p12 chr17: 37,730,015-37,730,017 , GRCh38.p12 chr17|NT_187614.1: 1,969,071-1,969,073 HNF1B
    nsv6130444insertion1nstd186human GRCh37 chr17: 36,982,202-36,982,233 , GRCh38.p12 chr17|NT_187614.1: 2,861,268-2,861,299 , GRCh38.p12 chr17: 38,825,949-38,825,980 MIR4727
    nsv6130051insertion1nstd186human GRCh37 chr17: 36,605,061-36,605,077 , GRCh38.p12 chr17: 38,448,817-38,448,833 , GRCh38.p12 chr17|NT_187614.1: 2,484,127-2,484,143 ARHGAP23, LOC101929494
    nsv6129538insertion1nstd186human GRCh37 chr17: 36,243,600-36,243,600 , GRCh38.p12 chr17: 37,883,980-37,883,980 , GRCh38.p12 chr17|NT_187614.1: 2,122,665-2,122,665 YWHAEP7
    nsv6129463mobile element insertion1nstd186human GRCh37 chr17: 34,272,166-34,272,217 , GRCh38.p12 chr17|NT_187614.1: 179,694-179,745 , GRCh38.p12 chr17: 35,945,162-35,945,213 0
    nsv6127764copy number variation1nstd186human GRCh37 chr17: 35,778,706-35,782,390 , GRCh38.p12 chr17: 37,418,621-37,422,284 , GRCh38.p12 chr17|NT_187614.1: 1,657,771-1,661,455 TADA2A
    nsv6125591copy number variation1nstd186human GRCh37 chr17: 35,796,584-35,797,613 , GRCh38.p12 chr17: 37,436,483-37,437,512 , GRCh38.p12 chr17|NT_187614.1: 1,675,649-1,676,678 TADA2A
    nsv6125323copy number variation1nstd186human GRCh37 chr17: 36,963,154-36,964,907 , GRCh38.p12 chr17: 38,806,901-38,808,654 , GRCh38.p12 chr17|NT_187614.1: 2,842,220-2,843,973 CWC25
    nsv6125030copy number variation1nstd186human GRCh37 chr17: 35,378,944-35,379,124 , GRCh38.p12 chr17: 37,021,645-37,021,825 , GRCh38.p12 chr17|NT_187614.1: 1,258,009-1,258,189 AATF
    nsv6123973copy number variation1nstd186human GRCh37 chr17: 36,168,947-36,169,329 , GRCh38.p12 chr17: 37,808,979-37,809,361 , GRCh38.p12 chr17|NT_187614.1: 2,048,012-2,048,394 LOC105371757
    nsv6117735mobile element insertion1nstd186human GRCh37 chr17: 36,208,683-36,208,689 , GRCh38.p12 chr17: 37,849,059-37,849,065 , GRCh38.p12 chr17|NT_187614.1: 2,087,748-2,087,754 YWHAEP7
    nsv6116954mobile element insertion1nstd186human GRCh37 chr17: 35,922,015-35,922,015 , GRCh38.p12 chr17: 37,561,913-37,561,913 , GRCh38.p12 chr17|NT_187614.1: 1,801,080-1,801,080 SYNRG
    nsv6116890copy number variation1nstd186human GRCh37 chr17: 36,285,525-36,301,525 , GRCh38.p12 chr17|NT_187614.1: 2,164,590-2,180,590 , TBC1D3E, 1 more genes
    nsv6114628mobile element insertion1nstd186human GRCh37 chr17: 35,492,978-35,492,978 , GRCh38.p12 chr17: 37,136,053-37,136,053 , GRCh38.p12 chr17|NT_187614.1: 1,372,043-1,372,043 ACACA
    nsv6114107mobile element insertion1nstd186human GRCh37 chr17: 35,869,998-35,870,009 , GRCh38.p12 chr17: 37,509,896-37,509,907 , GRCh38.p12 chr17|NT_187614.1: 1,749,063-1,749,074 DUSP14
    nsv6113849mobile element insertion1nstd186human GRCh37 chr17: 36,750,882-36,750,882 , GRCh38.p12 chr17: 38,594,629-38,594,629 , GRCh38.p12 chr17|NT_187614.1: 2,629,948-2,629,948 SRCIN1
    nsv6113043mobile element insertion1nstd186human GRCh37 chr17: 34,376,624-34,376,675 , GRCh38.p12 chr17: 36,049,260-36,049,311 , GRCh38.p12 chr17|NT_187661.1: 3,357-3,408 , GRCh38.p12 chr17|NT_187614.1: 284,152-284,203 LOC105371746, LOC107985068
    nsv6112791copy number variation1nstd102humanPathogenic GRCh37 chr17: 34,815,466-36,249,366 , GRCh38.p12 chr17|NT_187614.1: 694,556-2,128,431 , GRCh38.p12 chr17: 36,459,652-37,889,744 HNF1B, LOC107985031, 36 more genes
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