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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095934copy number variation1nstd102humanUncertain significance GRCh37 chr22: 26,142,492-27,026,451 , GRCh38.p12 chr22: 25,746,525-26,630,487 SRRD, TFIP11-DT, 18 more genes
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7069705inversion1nstd229human GRCh38 chr22: 26,003,361-26,660,401 , GRCh37.p13 chr22: 26,399,327-27,056,365 HPS4, LOC646216, 18 more genes
    nsv7064717inversion1nstd229human GRCh38 chr22: 25,959,817-26,562,327 , GRCh37.p13 chr22: 26,355,783-26,958,293 TPST2, SEZ6L, 15 more genes
    nsv7028873copy number variation1nstd229human GRCh38 chr22: 22,977,123-28,064,565 , GRCh37.p13 chr22: 23,319,297-28,460,553 LOC100652871, VPREB3, 132 more genes
    nsv6637977copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,614,429-29,847,680 , GRCh38.p12 chr22: 26,218,463-29,451,691 MIAT, LOC105372985, 65 more genes
    nsv6596913inversion1nstd223human GRCh38 chr22: 22,928,460-27,825,377 , GRCh37.p13 chr22: 23,270,636-28,221,365 LOC105372957, LOC105372980, 126 more genes
    nsv6134585copy number variation1nstd213human GRCh37 chr22: 26,860,000-27,590,001 , GRCh38.p12 chr22: 26,464,034-27,194,039 CRYBA4, CRYBB1, 18 more genes
    nsv6134584copy number variation1nstd213human GRCh37 chr22: 21,970,000-27,770,001 , GRCh38.p12 chr22: 21,615,711-27,374,040 ADORA2A, GRK3, 259 more genes
    nsv6129862insertion1nstd186human GRCh37 chr22: 26,949,615-26,949,642 , GRCh38.p12 chr22: 26,553,649-26,553,676 TPST2, MIR548J
    nsv6129233insertion1nstd186human GRCh37 chr22: 26,949,462-26,949,506 , GRCh38.p12 chr22: 26,553,496-26,553,540 MIR548J, TPST2
    nsv6111061insertion1nstd212human GRCh38 chr22: 26,553,560-26,553,560 , GRCh37.p13 chr22: 26,949,526-26,949,526 MIR548J, TPST2
    nsv5665032insertion1nstd207human GRCh38 chr22: 26,553,546-26,553,546 , GRCh37.p13 chr22: 26,949,512-26,949,512 TPST2, MIR548J
    nsv5547425insertion1nstd206human GRCh38 chr22: 26,553,649-26,553,676 , GRCh37.p13 chr22: 26,949,615-26,949,642 MIR548J, TPST2
    nsv5546005insertion1nstd206human GRCh38 chr22: 26,553,496-26,553,540 , GRCh37.p13 chr22: 26,949,462-26,949,506 MIR548J, TPST2
    nsv4763743insertion1nstd199human GRCh37 chr22: 26,949,510-26,949,510 , GRCh38.p12 chr22: 26,553,544-26,553,544 TPST2, MIR548J
    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
    nsv4676280copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,337,910-28,489,947 , GRCh38.p12 chr22: 25,941,943-28,093,959 LOC646216, MYO18B, 42 more genes
    nsv4676144copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-27,657,507 , GRCh38.p12 chr22: 16,408,173-27,261,546 LINC02891, IGLV4-69, 466 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 IGLV3-27, XKR3, 1082 more genes
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