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Items: 1 to 20 of 469

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv7141681insertion1nstd232human GRCh37.p13 chr2: 188,215,730-188,215,730 , GRCh38.p12 chr2: 187,351,003-187,351,003 CALCRL, CALCRL-AS1
    nsv7051925inversion1nstd229human GRCh38 chr2: 187,383,298-187,425,571 , GRCh37.p13 chr2: 188,248,025-188,290,298 CALCRL, GAPDHP59, 1 more genes
    nsv7038266inversion1nstd229human GRCh38 chr2: 187,371,855-187,386,944 , GRCh37.p13 chr2: 188,236,582-188,251,671 CALCRL-AS1, CALCRL
    nsv6697561copy number variation1nstd229human GRCh38 chr2: 187,342,301-187,344,700 , GRCh37.p13 chr2: 188,207,028-188,209,427 CALCRL, CALCRL-AS1
    nsv6696655copy number variation1nstd229human GRCh38 chr2: 187,401,383-187,405,245 , GRCh37.p13 chr2: 188,266,110-188,269,972 CALCRL-AS1, CALCRL
    nsv6695082copy number variation1nstd229human GRCh38 chr2: 187,152,304-187,457,976 , GRCh37.p13 chr2: 188,017,031-188,322,703 CALCRL, RNU6-989P, 2 more genes
    nsv6694715copy number variation1nstd229human GRCh38 chr2: 187,337,605-187,393,552 , GRCh37.p13 chr2: 188,202,332-188,258,279 CALCRL-AS1, CALCRL
    nsv6693850copy number variation1nstd229human GRCh38 chr2: 187,434,839-187,447,440 , GRCh37.p13 chr2: 188,299,566-188,312,167 CALCRL, CALCRL-AS1
    nsv6688417copy number variation1nstd229human GRCh38 chr2: 187,335,499-187,341,285 , GRCh37.p13 chr2: 188,200,226-188,206,012 CALCRL-AS1, CALCRL
    nsv6687099copy number variation1nstd229human GRCh38 chr2: 187,307,234-187,492,347 , GRCh37.p13 chr2: 188,171,961-188,357,074 CALCRL, CALCRL-AS1, 2 more genes
    nsv6685327copy number variation1nstd229human GRCh38 chr2: 187,350,991-187,351,298 , GRCh37.p13 chr2: 188,215,718-188,216,025 CALCRL, CALCRL-AS1
    nsv6684382copy number variation1nstd229human GRCh38 chr2: 187,366,076-187,375,220 , GRCh37.p13 chr2: 188,230,803-188,239,947 CALCRL, CALCRL-AS1
    nsv6682481copy number variation1nstd229human GRCh38 chr2: 187,075,291-187,428,337 , GRCh37.p13 chr2: 187,940,018-188,293,064 CALCRL-AS1, GAPDHP59, 3 more genes
    nsv6682014copy number variation1nstd229human GRCh38 chr2: 187,344,377-187,370,208 , GRCh37.p13 chr2: 188,209,104-188,234,935 CALCRL, CALCRL-AS1
    nsv6681351copy number variation1nstd229human GRCh38 chr2: 183,760,744-188,740,800 , GRCh37.p13 chr2: 184,625,471-189,605,527 MIR548AE1, LOC105373781, 42 more genes
    nsv6636571copy number variation1nstd102humanPathogenic GRCh37 chr2: 187,152,754-199,960,525 , GRCh38.p12 chr2: 186,288,027-199,095,802 GAPDHP59, OSGEPL1-AS1, 135 more genes
    nsv6636201copy number variation1nstd102humanUncertain significance GRCh37 chr2: 187,466,416-188,487,473 , GRCh38.p12 chr2: 186,601,689-187,622,746 CALCRL, ITGAV, 8 more genes
    nsv6554371inversion1nstd223human GRCh38 chr2: 187,340,515-187,341,138 , GRCh37.p13 chr2: 188,205,242-188,205,865 CALCRL, CALCRL-AS1
    nsv6548079inversion1nstd223human GRCh38 chr2: 178,157,654-187,669,944 , GRCh37.p13 chr2: 179,022,381-188,534,671 RNU7-104P, RN7SKP42, 90 more genes
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