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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5909028copy number variation1nstd209human GRCh38 chr11: 73,355,027-73,355,195 , GRCh37.p13 chr11: 73,066,072-73,066,240 ARHGEF17
    nsv5907717copy number variation1nstd209human GRCh38 chr11: 73,360,119-73,360,191 , GRCh37.p13 chr11: 73,071,164-73,071,236 ARHGEF17
    nsv5513618copy number variation1nstd206human GRCh38 chr11: 73,360,113-73,360,214 , GRCh37.p13 chr11: 73,071,158-73,071,259 ARHGEF17
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5342360translocation1nstd200human GRCh37 chr11: 73,066,075-73,066,075 , GRCh37 chr11: 73,066,241-73,066,241 , GRCh38.p12 chr11: 73,355,196-73,355,196 , GRCh38.p12 chr11: 73,355,030-73,355,030 ARHGEF17
    nsv5337100translocation1nstd200human GRCh37 chr11: 73,071,239-73,071,239 , GRCh37 chr11: 73,071,181-73,071,181 , GRCh38.p12 chr11: 73,360,194-73,360,194 , GRCh38.p12 chr11: 73,360,136-73,360,136 ARHGEF17
    nsv5269432copy number variation1nstd204human GRCh38.p13 chr11: 73,354,967-73,357,044 , GRCh37.p13 chr11: 73,066,012-73,068,089 ARHGEF17
    nsv5120553mobile element insertion1nstd203human GRCh38 chr11: 73,335,565-73,335,574 , GRCh37.p13 chr11: 73,046,610-73,046,619 ARHGEF17
    nsv4671759copy number variation1nstd186human GRCh37 chr11: 73,019,309-73,020,577 , GRCh38.p12 chr11: 73,308,264-73,309,532 ARHGEF17, ARHGEF17-AS1
    nsv4609247copy number variation1nstd183human GRCh37 chr11: 73,019,512-73,019,884 , GRCh38.p12 chr11: 73,308,467-73,308,839 ARHGEF17, ARHGEF17-AS1
    nsv4608138copy number variation1nstd183human GRCh37 chr11: 73,019,309-73,020,577 , GRCh38.p12 chr11: 73,308,264-73,309,532 ARHGEF17-AS1, ARHGEF17
    nsv4490231mobile element insertion1nstd166human GRCh37.p13 chr11: 73,025,792-73,025,792 , GRCh38.p12 chr11: 73,314,747-73,314,747 ARHGEF17
    nsv4480985mobile element insertion1nstd166human GRCh37.p13 chr11: 73,075,405-73,075,405 , GRCh38.p12 chr11: 73,364,360-73,364,360 ARHGEF17
    nsv4455208copy number variation1nstd102humanUncertain significance GRCh37 chr11: 72,998,686-73,156,844 , GRCh38.p12 chr11: 73,287,641-73,445,799 RELT, FAM168A, 3 more genes
    nsv4195400copy number variation1nstd166human GRCh37.p13 chr11: 72,962,000-73,045,800 , GRCh38.p12 chr11: 73,250,955-73,334,755 ARHGEF17-AS1, P2RY6, 2 more genes
    nsv4195157copy number variation1nstd166human GRCh37.p13 chr11: 73,071,181-73,071,239 , GRCh38.p12 chr11: 73,360,136-73,360,194 ARHGEF17
    nsv4192642copy number variation1nstd166human GRCh37.p13 chr11: 73,043,304-73,044,406 , GRCh38.p12 chr11: 73,332,259-73,333,361 ARHGEF17
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
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