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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095117copy number variation1nstd102humanPathogenic GRCh37 chr16: 89,712,474-89,866,066 , GRCh38.p12 chr16: 89,646,066-89,799,658 FANCA, CHMP1A, 7 more genes
    nsv7095062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,556,653-89,851,392 , GRCh38.p12 chr16: 89,490,245-89,784,984 SNORD68, CHMP1A, 15 more genes
    nsv7095060copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,167,090-89,883,023 , GRCh38.p12 chr16: 89,100,682-89,816,615 VPS9D1, ZNF276, 26 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
    nsv7073763inversion1nstd229human GRCh38 chr16: 89,536,886-89,757,402 , GRCh37.p13 chr16: 89,603,294-89,823,810 SPATA33, SNORD68, 12 more genes
    nsv6997823copy number variation1nstd229human GRCh38 chr16: 89,630,157-89,815,080 , GRCh37.p13 chr16: 89,696,565-89,881,488 VPS9D1-AS1, CDK10, 8 more genes
    nsv6988144copy number variation1nstd229human GRCh38 chr16: 89,658,140-89,827,515 , GRCh37.p13 chr16: 89,724,548-89,893,923 ZNF276, VPS9D1, 8 more genes
    nsv6987256copy number variation1nstd229human GRCh38 chr16: 89,673,407-89,705,832 , GRCh37.p13 chr16: 89,739,815-89,772,240 VPS9D1, LINC02166, 2 more genes
    nsv6985866copy number variation1nstd229human GRCh38 chr16: 89,473,541-89,719,269 , GRCh37.p13 chr16: 89,539,949-89,785,677 ANKRD11, SPATA33, 14 more genes
    nsv6985702copy number variation1nstd229human GRCh38 chr16: 89,701,079-89,779,271 , GRCh37.p13 chr16: 89,767,487-89,845,679 SPATA2L, FANCA, 3 more genes
    nsv6982338copy number variation1nstd229human GRCh38 chr16: 89,606,222-89,817,329 , GRCh37.p13 chr16: 89,672,630-89,883,737 SPATA33, CHMP1A, 8 more genes
    nsv6981920copy number variation1nstd229human GRCh38 chr16: 89,589,701-89,705,900 , GRCh37.p13 chr16: 89,656,109-89,772,308 SPATA33, CHMP1A, 6 more genes
    nsv6980515copy number variation1nstd229human GRCh38 chr16: 89,669,085-89,719,800 , GRCh37.p13 chr16: 89,735,493-89,786,208 CDK10, VPS9D1, 5 more genes
    nsv6978455copy number variation1nstd229human GRCh38 chr16: 89,690,629-89,695,392 , GRCh37.p13 chr16: 89,757,037-89,761,800 CDK10, SPATA2L
    nsv6638038copy number variation1nstd102humanUncertain significance GRCh37 chr16: 89,662,422-89,895,938 , GRCh38.p12 chr16: 89,596,014-89,829,530 SPATA2L, LINC02166, 10 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
    nsv6581057inversion1nstd223human GRCh38 chr16: 89,666,964-89,753,078 , GRCh37.p13 chr16: 89,733,372-89,819,486 FANCA, CDK10, 6 more genes
    nsv6580580inversion1nstd223human GRCh38 chr16: 89,636,100-89,730,767 , GRCh37.p13 chr16: 89,702,508-89,797,175 DPEP1, CHMP1A, 7 more genes
    nsv6513036copy number variation1nstd223human GRCh38 chr16: 89,607,402-89,702,833 , GRCh37.p13 chr16: 89,673,810-89,769,241 LINC02166, DPEP1, 4 more genes
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