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Items: 1 to 20 of 211

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097159copy number variation2nstd102humanUncertain significance GRCh37 chr5: 73,980,960-75,008,762 , GRCh38.p12 chr5: 74,685,135-75,712,937 NSA2, RNU6-680P, 22 more genes
    nsv7045293inversion1nstd229human GRCh38 chr5: 73,247,847-76,069,477 , GRCh37.p13 chr5: 72,543,674-75,365,302 LOC107986423, NSA2, 48 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv6775060copy number variation1nstd229human GRCh38 chr5: 74,857,669-74,857,696 , GRCh37.p13 chr5: 74,153,494-74,153,521 FAM169A
    nsv6770040copy number variation1nstd229human GRCh38 chr5: 74,748,601-74,961,100 , GRCh37.p13 chr5: 74,044,426-74,256,925 LOC105379039, LOC100131411, 8 more genes
    nsv6770014copy number variation1nstd229human GRCh38 chr5: 74,697,748-74,779,149 , GRCh37.p13 chr5: 73,993,573-74,074,974 HEXB, RNU6-658P, 4 more genes
    nsv6766203copy number variation1nstd229human GRCh38 chr5: 74,807,885-74,810,293 , GRCh37.p13 chr5: 74,103,710-74,106,118 FAM169A
    nsv6760563copy number variation1nstd229human GRCh38 chr5: 74,745,521-74,779,428 , GRCh37.p13 chr5: 74,041,346-74,075,253 GFM2, FAM169A, 2 more genes
    nsv6760125copy number variation1nstd229human GRCh38 chr5: 74,841,683-74,843,169 , GRCh37.p13 chr5: 74,137,508-74,138,994 FAM169A
    nsv6566266inversion1nstd223human GRCh38 chr5: 74,819,201-74,820,028 , GRCh37.p13 chr5: 74,115,026-74,115,853 FAM169A
    nsv6562546inversion1nstd223human GRCh38 chr5: 74,859,110-74,859,359 , GRCh37.p13 chr5: 74,154,935-74,155,184 FAM169A
    nsv6414358copy number variation1nstd223human GRCh38 chr5: 74,825,305-74,825,958 , GRCh37.p13 chr5: 74,121,130-74,121,783 FAM169A
    nsv6414089copy number variation1nstd223human GRCh38 chr5: 74,786,108-74,792,342 , GRCh37.p13 chr5: 74,081,933-74,088,167 FAM169A
    nsv6405230copy number variation1nstd223human GRCh38 chr5: 74,833,822-74,834,216 , GRCh37.p13 chr5: 74,129,647-74,130,041 FAM169A
    nsv6403414copy number variation1nstd223human GRCh38 chr5: 74,770,101-74,776,600 , GRCh37.p13 chr5: 74,065,926-74,072,425 FAM169A, NSA2
    nsv6402456copy number variation1nstd223human GRCh38 chr5: 74,776,701-74,778,300 , GRCh37.p13 chr5: 74,072,526-74,074,125 NSA2, FAM169A, 1 more genes
    nsv6400769copy number variation1nstd223human GRCh38 chr5: 74,824,042-74,824,453 , GRCh37.p13 chr5: 74,119,867-74,120,278 FAM169A
    nsv6399568copy number variation1nstd223human GRCh38 chr5: 74,777,688-74,778,727 , GRCh37.p13 chr5: 74,073,513-74,074,552 NSA2, FAM169A, 1 more genes
    nsv6398023copy number variation1nstd223human GRCh38 chr5: 74,777,601-74,779,700 , GRCh37.p13 chr5: 74,073,426-74,075,525 RNU6-1330P, FAM169A, 1 more genes
    nsv6397228copy number variation1nstd223human GRCh38 chr5: 74,831,467-74,831,902 , GRCh37.p13 chr5: 74,127,292-74,127,727 FAM169A
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