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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048415inversion1nstd229human GRCh38 chr2: 75,781,048-78,603,127 , GRCh37.p13 chr2: 76,008,174-78,830,253 LOC101927948, RN7SKP164, 20 more genes
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv6690545copy number variation1nstd229human GRCh38 chr2: 77,891,704-78,052,196 , GRCh37.p13 chr2: 78,118,830-78,279,322 LOC105374816, LOC105374817, 3 more genes
    nsv6689763copy number variation1nstd229human GRCh38 chr2: 77,909,697-77,933,984 , GRCh37.p13 chr2: 78,136,823-78,161,110 LOC101927967, LOC105374817, 1 more genes
    nsv6688471copy number variation1nstd229human GRCh38 chr2: 77,792,759-78,415,712 , GRCh37.p13 chr2: 78,019,885-78,642,838 LOC101927948, LOC101927967, 6 more genes
    nsv6686826copy number variation1nstd229human GRCh38 chr2: 77,903,642-77,923,090 , GRCh37.p13 chr2: 78,130,768-78,150,216 LOC101927967, LINC01851, 1 more genes
    nsv6683597copy number variation1nstd229human GRCh38 chr2: 77,778,262-78,615,654 , GRCh37.p13 chr2: 78,005,388-78,842,780 CYCSP6, LOC105374817, 9 more genes
    nsv6681956copy number variation1nstd229human GRCh38 chr2: 77,915,058-77,993,750 , GRCh37.p13 chr2: 78,142,184-78,220,876 LINC01851, LOC105374816, 3 more genes
    nsv6678348copy number variation1nstd229human GRCh38 chr2: 77,819,076-78,018,447 , GRCh37.p13 chr2: 78,046,202-78,245,573 SNAR-H, LOC101927967, 3 more genes
    nsv6636900copy number variation1nstd102humanUncertain significance GRCh37 chr2: 77,324,190-78,188,451 , GRCh38.p12 chr2: 77,097,064-77,961,325 LRRTM4, LOC105374817, 5 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628346copy number variation1nstd224human GRCh37 chr2: 78,027,063-78,185,777 , GRCh38.p12 chr2: 77,799,937-77,958,651 SNAR-H, LINC01851, 2 more genes
    nsv6628149copy number variation1nstd224human GRCh37 chr2: 78,102,968-78,342,416 , GRCh38.p12 chr2: 77,875,842-78,115,290 SNAR-H, LINC01851, 4 more genes
    nsv6628146copy number variation1nstd224human GRCh37 chr2: 77,292,449-78,190,949 , GRCh38.p12 chr2: 77,065,323-77,963,823 LRRTM4, RPL38P2, 5 more genes
    nsv6545236inversion1nstd223human GRCh38 chr2: 75,781,046-78,603,129 , GRCh37.p13 chr2: 76,008,172-78,830,255 LOC101927948, LOC100421651, 20 more genes
    nsv6348952copy number variation1nstd223human GRCh38 chr2: 77,915,058-77,993,755 , GRCh37.p13 chr2: 78,142,184-78,220,881 LOC105374817, LINC01851, 3 more genes
    nsv6347359copy number variation1nstd223human GRCh38 chr2: 77,914,001-77,915,600 , GRCh37.p13 chr2: 78,141,127-78,142,726 LOC101927967, LINC01851
    nsv6341399copy number variation1nstd223human GRCh38 chr2: 77,890,570-78,023,195 , GRCh37.p13 chr2: 78,117,696-78,250,321 LOC105374817, LINC01851, 3 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
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