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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095127copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,094,024-90,109,753 , GRCh38.p12 chr16: 90,027,616-90,043,345 URAHP, GAS8-AS1, 1 more genes
    nsv7094949copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,094,024-90,099,352 , GRCh38.p12 chr16: 90,027,616-90,032,944 GAS8, GAS8-AS1
    nsv7094948copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,089,130-90,106,937 , GRCh38.p12 chr16: 90,022,722-90,040,529 URAHP, GAS8-AS1, 1 more genes
    nsv7094940copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,611,036-90,106,937 , GRCh38.p12 chr16: 89,544,628-90,040,529 SPATA2L, LINC02166, 25 more genes
    nsv7094699copy number variation2nstd102humanUncertain significance GRCh37 chr16: 87,636,753-90,109,753 , GRCh38.p12 chr16: 87,603,147-90,043,345 HSALR1, LOC105371412, 87 more genes
    nsv7068471inversion1nstd229human GRCh38 chr16: 90,012,838-90,034,579 , GRCh37.p13 chr16: 90,079,246-90,100,987 GAS8, DBNDD1, 1 more genes
    nsv6994365copy number variation1nstd229human GRCh38 chr16: 90,002,953-90,080,293 , GRCh37.p13 chr16: 90,069,361-90,146,701 PRDM7, GAS8-AS1, 3 more genes
    nsv6992552copy number variation1nstd229human GRCh38 chr16: 90,014,227-90,040,253 , GRCh37.p13 chr16: 90,080,635-90,106,661 GAS8-AS1, GAS8, 2 more genes
    nsv6986741copy number variation1nstd229human GRCh38 chr16: 90,024,001-90,035,900 , GRCh37.p13 chr16: 90,090,409-90,102,308 GAS8-AS1, GAS8
    nsv6982491copy number variation1nstd229human GRCh38 chr16: 90,021,014-90,043,596 , GRCh37.p13 chr16: 90,087,422-90,110,004 URAHP, GAS8-AS1, 1 more genes
    nsv6979877copy number variation1nstd229human GRCh38 chr16: 89,999,531-90,055,074 , GRCh37.p13 chr16: 90,065,939-90,121,482 PRDM7, DBNDD1, 4 more genes
    nsv6634465copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 71,610,276-90,354,753 , GRCh38.p12 chr16: 71,576,373-90,228,345 AP1G1, AFG3L1P, 349 more genes
    nsv6624189copy number variation1nstd224human GRCh37 chr16: 90,084,561-90,142,260 , GRCh38.p12 chr16: 90,018,153-90,075,852 GAS8, PRDM7, 3 more genes
    nsv6624031copy number variation1nstd224human GRCh37 chr16: 90,079,927-90,130,136 , GRCh38.p12 chr16: 90,013,519-90,063,728 GAS8-AS1, URAHP, 3 more genes
    nsv6623804copy number variation1nstd224human GRCh37 chr16: 90,079,534-90,130,152 , GRCh38.p12 chr16: 90,013,126-90,063,744 DBNDD1, GAS8, 3 more genes
    nsv6497381copy number variation1nstd223human GRCh38 chr16: 90,020,213-90,097,271 , GRCh37.p13 chr16: 90,086,621-90,163,679 GAS8, DBNDD1, 4 more genes
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6310116copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,094,024-90,094,150 , GRCh38.p12 chr16: 90,027,616-90,027,742 GAS8, GAS8-AS1
    nsv6309957copy number variation1nstd102humanPathogenic GRCh37 chr16: 90,089,130-90,094,150 , GRCh38.p12 chr16: 90,022,722-90,027,742 GAS8, GAS8-AS1
    nsv6291643copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,337,891-90,155,062 , GRCh38.p12 chr16: 89,271,483-90,088,654 DBNDD1, AFG3L1P, 34 more genes
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