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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 CSF2RBP1, H1-0, 80 more genes
    nsv7078067inversion1nstd229human GRCh38 chr22: 30,287,061-38,012,264 , GRCh37.p13 chr22: 30,683,050-38,408,271 LINC02885, RN7SL20P, 203 more genes
    nsv7072766inversion1nstd229human GRCh38 chr22: 35,603,617-39,341,195 , GRCh37.p13 chr22: 35,999,664-39,737,200 APOL5, MTATP6P20, 132 more genes
    nsv7065500inversion1nstd229human GRCh38 chr22: 29,260,563-37,652,385 , GRCh37.p13 chr22: 29,656,552-38,048,392 RFPL1, PATZ1, 217 more genes
    nsv7064066inversion1nstd229human GRCh38 chr22: 34,920,312-39,418,308 , GRCh37.p13 chr22: 35,316,302-39,814,313 LOC112268295, APOBEC3B-AS1, 150 more genes
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7059210inversion1nstd229human GRCh38 chr22: 35,603,611-39,337,136 , GRCh37.p13 chr22: 35,999,658-39,733,141 MTCO2P20, RPS29P31, 132 more genes
    nsv7032615copy number variation1nstd229human GRCh38 chr22: 37,566,001-37,572,900 , GRCh37.p13 chr22: 37,962,008-37,968,907 LGALS2, CDC42EP1
    nsv7028872copy number variation1nstd229human GRCh38 chr22: 37,555,648-37,575,652 , GRCh37.p13 chr22: 37,951,655-37,971,659 CDC42EP1, LGALS2
    nsv7025536copy number variation1nstd229human GRCh38 chr22: 37,287,222-37,834,908 , GRCh37.p13 chr22: 37,683,263-38,230,915 GGA1, GALR3, 19 more genes
    nsv7024995copy number variation1nstd229human GRCh38 chr22: 37,460,835-37,706,454 , GRCh37.p13 chr22: 37,856,873-38,102,461 CARD10, MFNG, 10 more genes
    nsv7022186copy number variation1nstd229human GRCh38 chr22: 37,474,145-37,706,268 , GRCh37.p13 chr22: 37,870,183-38,102,275 TRIOBP, SH3BP1, 10 more genes
    nsv6627104copy number variation1nstd224human GRCh37 chr22: 37,929,759-38,003,624 , GRCh38.p12 chr22: 37,533,752-37,607,617 LGALS2, CDC42EP1, 1 more genes
    nsv6544785copy number variation1nstd223human GRCh38 chr22: 37,556,154-37,577,412 , GRCh37.p13 chr22: 37,952,161-37,973,419 LGALS2, CDC42EP1
    nsv6541398copy number variation1nstd223human GRCh38 chr22: 37,543,538-37,586,521 , GRCh37.p13 chr22: 37,939,545-37,982,528 CDC42EP1, LGALS2
    nsv6540218copy number variation1nstd223human GRCh38 chr22: 37,287,222-37,834,905 , GRCh37.p13 chr22: 37,683,263-38,230,912 GALR3, LOC102724378, 19 more genes
    nsv6134213copy number variation1nstd213human GRCh37 chr22: 37,470,000-39,980,001 , GRCh38.p12 chr22: 37,073,960-39,583,996 ATF4, COX5BP7, 98 more genes
    nsv6134212copy number variation1nstd213human GRCh37 chr22: 36,430,000-39,960,001 , GRCh38.p12 chr22: 36,033,952-39,563,996 ATF4, COX5BP7, 133 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
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