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Items: 1 to 20 of 189

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112800copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,977-21,463,189 , GRCh38.p12 chr22: 18,339,130-21,108,900 MIR4761, TUBA3FP, 124 more genes
    nsv6112793copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,693-21,465,485 , GRCh38.p12 chr22: 18,339,130-21,111,196 THAP7, LOC100129262, 125 more genes
    nsv6112789copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,730,996-21,465,342 , GRCh38.p12 chr22: 20,376,706-21,111,053 IGLL4P, CRKL, 39 more genes
    nsv6112781copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,841,374-21,465,101 , GRCh38.p12 chr22: 18,339,130-21,110,812 SEPTIN5, RNU6-225P, 125 more genes
    nsv6112779copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,571-21,464,697 , GRCh38.p12 chr22: 18,339,130-21,110,408 PRODH, MIR3618, 124 more genes
    nsv5980456copy number variation1nstd102humanUncertain significance GRCh37 chr22: 20,737,912-21,465,659 , GRCh38.p12 chr22: 20,383,622-21,111,370 KRT18P5, SLC9A3P2, 39 more genes
    nsv5980452copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,969-21,462,658 , GRCh38.p12 chr22: 18,339,130-21,108,369 LINC01637, BCRP7, 124 more genes
    nsv5967784inversion1nstd209human GRCh38 chr22: 20,337,735-21,327,040 , GRCh37.p13 chr22: 20,325,258-21,681,329 , CRKL, 49 more genes
    nsv5673274copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,563,420 , GRCh38.p12 chr22: 18,339,130-21,209,131 UFD1-AS1, LOC100129254, 129 more genes
    nsv5673185copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,571,027 , GRCh38.p12 chr22: 18,339,130-21,216,738 CCDC188, LOC107987325, 129 more genes
    nsv5670785inversion1nstd207human GRCh38 chr22: 18,746,351-21,188,291 , GRCh37.p13 chr22: 18,733,864-21,542,580 , ARVCF, 114 more genes
    nsv5546016copy number variation1nstd206human GRCh38 chr22: 20,689,282-21,312,400 , GRCh37.p13 chr22: 21,043,570-21,666,689 , BCRP2, 30 more genes
    nsv5535972copy number variation1nstd206human GRCh38 chr22: 20,679,564-21,209,564 , GRCh37.p13 chr22: 21,033,852-21,563,853 , PI4KA, 26 more genes
    nsv5381807copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,886,915-21,461,017 , GRCh38.p12 chr22: 18,339,130-21,106,728 BCRP5, TSSK2, 124 more genes
    nsv5381313copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,490-21,463,730 , GRCh38.p12 chr22: 18,339,130-21,109,441 SERPIND1, CA15P1, 124 more genes
    nsv5381148copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,886,915-21,463,730 , GRCh38.p12 chr22: 18,339,130-21,109,441 MIR3618, SMPD4P1, 124 more genes
    nsv5380708copy number variation1nstd208human GRCh37 chr22: 18,910,000-21,459,999 , GRCh38.p12 chr22: 18,339,130-21,105,710 , ARVCF, 126 more genes
    nsv5380707copy number variation1nstd208human GRCh37 chr22: 18,912,300-21,465,400 , GRCh38.p12 chr22: 18,339,130-21,111,111 , ARVCF, 127 more genes
    nsv5299960copy number variation1nstd204human GRCh38.p13 chr22: 20,689,301-21,112,100 , GRCh37.p13 chr22: 21,043,589-21,466,389 SERPIND1, LOC112268300, 21 more genes
    nsv5297360copy number variation1nstd204human GRCh38.p13 chr22: 21,042,905-21,086,252 , GRCh37.p13 chr22: 21,397,194-21,440,541 LRRC74B, P2RX6P, 2 more genes
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