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Items: 1 to 20 of 342

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140740insertion1nstd232human GRCh37.p13 chr1: 223,521,087-223,521,087 , GRCh38.p12 chr1: 223,347,745-223,347,745 SUSD4
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7044193inversion1nstd229human GRCh38 chr1: 223,313,164-223,313,244 , GRCh37.p13 chr1: 223,486,506-223,486,586 SUSD4
    nsv6677682copy number variation1nstd229human GRCh38 chr1: 223,252,341-223,258,784 , GRCh37.p13 chr1: 223,425,683-223,432,126 SUSD4
    nsv6675007copy number variation1nstd229human GRCh38 chr1: 222,711,079-223,231,899 , GRCh37.p13 chr1: 222,884,421-223,405,241 LOC102724046, FAM177B, 8 more genes
    nsv6670011copy number variation1nstd229human GRCh38 chr1: 223,299,894-223,304,855 , GRCh37.p13 chr1: 223,473,236-223,478,197 SUSD4
    nsv6669845copy number variation1nstd229human GRCh38 chr1: 223,304,750-223,316,753 , GRCh37.p13 chr1: 223,478,092-223,490,095 SUSD4
    nsv6667844copy number variation1nstd229human GRCh38 chr1: 223,259,009-223,259,106 , GRCh37.p13 chr1: 223,432,351-223,432,448 SUSD4
    nsv6666791copy number variation1nstd229human GRCh38 chr1: 223,268,595-223,276,418 , GRCh37.p13 chr1: 223,441,937-223,449,760 SUSD4
    nsv6666377copy number variation1nstd229human GRCh38 chr1: 223,327,387-223,340,497 , GRCh37.p13 chr1: 223,500,729-223,513,839 SUSD4
    nsv6666195copy number variation1nstd229human GRCh38 chr1: 223,226,616-223,226,978 , GRCh37.p13 chr1: 223,399,958-223,400,320 SUSD4
    nsv6666070copy number variation1nstd229human GRCh38 chr1: 223,330,522-223,330,883 , GRCh37.p13 chr1: 223,503,864-223,504,225 SUSD4
    nsv6662256copy number variation1nstd229human GRCh38 chr1: 223,348,816-223,348,955 , GRCh37.p13 chr1: 223,522,158-223,522,297 SUSD4
    nsv6660716copy number variation1nstd229human GRCh38 chr1: 223,262,993-223,269,308 , GRCh37.p13 chr1: 223,436,335-223,442,650 SUSD4
    nsv6659070copy number variation1nstd229human GRCh38 chr1: 223,070,801-223,236,000 , GRCh37.p13 chr1: 223,244,143-223,409,342 LOC107985323, LOC102724046, 2 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6626172copy number variation1nstd224human GRCh37 chr1: 223,408,378-223,438,771 , GRCh38.p12 chr1: 223,235,036-223,265,429 SUSD4
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
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