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Items: 1 to 20 of 150

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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
    nsv7076272inversion1nstd229human GRCh38 chr22: 26,419,869-26,429,017 , GRCh37.p13 chr22: 26,815,835-26,824,983 LOC646216, ASPHD2
    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
    nsv7031452copy number variation1nstd229human GRCh38 chr22: 26,437,001-26,459,700 , GRCh37.p13 chr22: 26,832,967-26,855,666 ASPHD2, HPS4
    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
    nsv7025198copy number variation1nstd229human GRCh38 chr22: 26,444,893-26,447,431 , GRCh37.p13 chr22: 26,840,859-26,843,397 ASPHD2, HPS4
    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
    nsv6283237copy number variation1nstd214human GRCh38 chr22: 26,427,360-26,427,497 , GRCh37.p13 chr22: 26,823,326-26,823,463 ASPHD2
    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
    nsv6125258copy number variation1nstd186human GRCh37 chr22: 26,823,474-26,823,774 , GRCh38.p12 chr22: 26,427,508-26,427,808 ASPHD2
    nsv6110543insertion1nstd212human GRCh38 chr22: 26,427,784-26,427,784 , GRCh37.p13 chr22: 26,823,750-26,823,750 ASPHD2
    nsv6059375copy number variation1nstd212human GRCh38 chr22: 26,427,458-26,427,725 , GRCh37.p13 chr22: 26,823,424-26,823,691 ASPHD2
    nsv5591444copy number variation1nstd207human GRCh38 chr22: 26,427,360-26,427,635 , GRCh37.p13 chr22: 26,823,326-26,823,601 ASPHD2
    nsv5547601copy number variation1nstd206human GRCh38 chr22: 26,427,508-26,427,808 , GRCh37.p13 chr22: 26,823,474-26,823,774 ASPHD2
    nsv5390562copy number variation1nstd186human GRCh37 chr22: 26,823,419-26,823,615 , GRCh38.p12 chr22: 26,427,453-26,427,649 ASPHD2
    nsv5327597copy number variation1nstd204human GRCh38.p13 chr22: 26,427,198-26,427,821 , GRCh37.p13 chr22: 26,823,164-26,823,787 ASPHD2
    nsv5285364copy number variation1nstd204human GRCh38.p13 chr22: 26,427,401-26,427,700 , GRCh37.p13 chr22: 26,823,367-26,823,666 ASPHD2
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