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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139700copy number variation1nstd232human GRCh37.p13 chr22: 40,403,334-40,403,434 , GRCh38.p12 chr22: 40,007,330-40,007,430 FAM83F
    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
    nsv7036210copy number variation1nstd229human GRCh38 chr22: 40,026,100-40,029,486 , GRCh37.p13 chr22: 40,422,104-40,425,490 FAM83F
    nsv7035567copy number variation1nstd229human GRCh38 chr22: 40,018,246-40,023,231 , GRCh37.p13 chr22: 40,414,250-40,419,235 FAM83F
    nsv7034268copy number variation1nstd229human GRCh38 chr22: 39,981,218-40,017,626 , GRCh37.p13 chr22: 40,377,222-40,413,630 FAM83F
    nsv7030683copy number variation1nstd229human GRCh38 chr22: 39,997,541-40,001,281 , GRCh37.p13 chr22: 40,393,545-40,397,285 FAM83F
    nsv7029820copy number variation1nstd229human GRCh38 chr22: 40,004,878-40,008,457 , GRCh37.p13 chr22: 40,400,882-40,404,461 FAM83F
    nsv7028909copy number variation1nstd229human GRCh38 chr22: 40,005,478-40,018,778 , GRCh37.p13 chr22: 40,401,482-40,414,782 FAM83F
    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
    nsv7026516copy number variation1nstd229human GRCh38 chr22: 40,015,001-40,019,600 , GRCh37.p13 chr22: 40,411,005-40,415,604 FAM83F
    nsv7022230copy number variation1nstd229human GRCh38 chr22: 40,004,160-40,007,132 , GRCh37.p13 chr22: 40,400,164-40,403,136 FAM83F
    nsv6638050copy number variation1nstd102humanPathogenic GRCh37 chr22: 40,131,240-41,556,564 , GRCh38.p12 chr22: 39,735,235-41,160,560 GRAP2, UQCRFS1P1, 32 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
    nsv6626954copy number variation1nstd224human GRCh37 chr22: 39,907,318-40,563,020 , GRCh38.p12 chr22: 39,511,313-40,167,016 ATF4, MIEF1, 12 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
    nsv6546586copy number variation1nstd223human GRCh38 chr22: 40,004,159-40,007,131 , GRCh37.p13 chr22: 40,400,163-40,403,135 FAM83F
    nsv6540105copy number variation1nstd223human GRCh38 chr22: 39,997,541-40,001,275 , GRCh37.p13 chr22: 40,393,545-40,397,279 FAM83F
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