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Items: 1 to 20 of 303

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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
    nsv7094950copy number variation1nstd102humanUncertain significance GRCh37 chr16: 90,106,688-90,109,753 , GRCh38.p12 chr16: 90,040,280-90,043,345 GAS8, URAHP
    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
    nsv6996048copy number variation1nstd229human GRCh38 chr16: 90,047,824-90,054,560 , GRCh37.p13 chr16: 90,114,232-90,120,968 URAHP
    nsv6995830copy number variation1nstd229human GRCh38 chr16: 90,036,665-90,060,759 , GRCh37.p13 chr16: 90,103,073-90,127,167 PRDM7, GAS8, 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
    nsv6988665copy number variation1nstd229human GRCh38 chr16: 90,047,233-90,063,219 , GRCh37.p13 chr16: 90,113,641-90,129,627 URAHP, PRDM7
    nsv6987316copy number variation1nstd229human GRCh38 chr16: 90,047,276-90,055,141 , GRCh37.p13 chr16: 90,113,684-90,121,549 URAHP, PRDM7
    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
    nsv6981628copy number variation1nstd229human GRCh38 chr16: 90,042,201-90,084,500 , GRCh37.p13 chr16: 90,108,609-90,150,908 GAS8, URAHP, 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
    nsv6506181copy number variation1nstd223human GRCh38 chr16: 90,041,419-90,045,850 , GRCh37.p13 chr16: 90,107,827-90,112,258 GAS8, URAHP
    nsv6505679copy number variation1nstd223human GRCh38 chr16: 90,045,240-90,056,340 , GRCh37.p13 chr16: 90,111,648-90,122,748 URAHP, GAS8, 1 more genes
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