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Items: 1 to 20 of 148

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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
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 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
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7030153copy number variation1nstd229human GRCh38 chr22: 41,228,735-41,247,128 , GRCh37.p13 chr22: 41,624,739-41,643,132 L3MBTL2, RANGAP1, 1 more genes
    nsv7029911copy number variation1nstd229human GRCh38 chr22: 41,184,501-41,252,200 , GRCh37.p13 chr22: 41,580,505-41,648,204 LOC646927, L3MBTL2-AS1, 6 more genes
    nsv7029110copy number variation1nstd229human GRCh38 chr22: 41,227,203-41,234,947 , GRCh37.p13 chr22: 41,623,207-41,630,951 L3MBTL2, CHADL
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7026524copy number variation1nstd229human GRCh38 chr22: 41,240,658-41,243,414 , GRCh37.p13 chr22: 41,636,662-41,639,418 RANGAP1, CHADL
    nsv7023452copy number variation1nstd229human GRCh38 chr22: 41,183,197-41,231,815 , GRCh37.p13 chr22: 41,579,201-41,627,819 LOC646927, L3MBTL2, 4 more genes
    nsv7022955copy number variation1nstd229human GRCh38 chr22: 41,175,146-41,333,607 , GRCh37.p13 chr22: 41,571,150-41,729,611 EP300, MIR6889, 8 more genes
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6550804copy number variation1nstd223human GRCh38 chr22: 41,183,197-41,231,810 , GRCh37.p13 chr22: 41,579,201-41,627,814 L3MBTL2-AS1, EP300-AS1, 4 more genes
    nsv6548196copy number variation1nstd223human GRCh38 chr22: 41,236,401-41,241,200 , GRCh37.p13 chr22: 41,632,405-41,637,204 CHADL
    nsv6544096copy number variation1nstd223human GRCh38 chr22: 41,227,203-41,234,947 , GRCh37.p13 chr22: 41,623,207-41,630,951 CHADL, L3MBTL2
    nsv6538638copy number variation1nstd223human GRCh38 chr22: 41,232,201-41,233,300 , GRCh37.p13 chr22: 41,628,205-41,629,304 CHADL
    nsv6536307copy number variation1nstd223human GRCh38 chr22: 41,240,926-41,244,788 , GRCh37.p13 chr22: 41,636,930-41,640,792 CHADL, RANGAP1
    nsv6311137copy number variation1nstd102humanUncertain significance GRCh37 chr22: 41,277,754-43,089,957 , GRCh38.p12 chr22: 40,881,750-42,693,951 RRP7A, OGFRP1, 79 more genes
    nsv6252156mobile element insertion1nstd215human GRCh38 chr22: 41,242,183-41,242,183 , GRCh37.p13 chr22: 41,638,187-41,638,187 CHADL
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