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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5041509inversion1nstd200human GRCh38 chr6: 91,773,985-92,844,182 , GRCh37.p13 chr6: 92,483,703-93,553,900 LOC100129847, RPL5P19, 3 more genes
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4942114copy number variation1nstd200human GRCh38 chr6: 91,626,944-92,323,638 , GRCh37.p13 chr6: 92,336,662-93,033,356 LOC100129847, RPL5P19, 7 more genes
    nsv4680814copy number variation1nstd189human GRCh37.p13 chr6: 91,959,681-92,636,081 , GRCh38.p12 chr6: 91,249,963-91,926,363 LOC100129847, MIR4643, 7 more genes
    nsv4616196copy number variation1nstd183human GRCh37 chr6: 92,328,392-93,210,400 , GRCh38.p12 chr6: 91,618,674-92,500,682 LOC100129847, RPL5P19, 7 more genes
    nsv4611910copy number variation1nstd183human GRCh37 chr6: 92,280,070-92,530,860 , GRCh38.p12 chr6: 91,570,352-91,821,142 LOC100129847, CASC6, 5 more genes
    nsv4603764copy number variation1nstd183human GRCh37 chr6: 91,388,110-94,538,696 , GRCh38.p12 chr6: 90,678,391-93,828,978 ATF1P1, LOC107986624, 18 more genes
    nsv4456405copy number variation1nstd102humanUncertain significance GRCh37 chr6: 87,627,836-93,698,486 , GRCh38.p12 chr6: 86,918,118-92,988,768 MIR4643, LOC107986625, 82 more genes
    nsv4455227copy number variation1nstd102humanUncertain significance GRCh37 chr6: 88,783,642-96,282,103 , GRCh38.p12 chr6: 88,073,924-95,834,227 MDN1, DNAJC19P6, 65 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4147935copy number variation1nstd166human GRCh37.p13 chr6: 92,336,662-93,033,356 , GRCh38.p12 chr6: 91,626,944-92,323,638 LOC100129847, RPL5P19, 7 more genes
    nsv3969533copy number variation1nstd168human GRCh38 chr6: 91,811,195-91,852,596 , GRCh37.p13 chr6: 92,520,913-92,562,314 LOC100129847
    nsv3924402copy number variation1nstd102humanUncertain significance GRCh38 chr6: 90,888,950-93,582,834 , GRCh37 chr6: 91,598,668-94,292,552 , NCBI36 chr6: 91,655,389-94,349,273 CASC6, MTCO1P56, 17 more genes
    nsv3923528copy number variation1nstd102humanPathogenic NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189 RNU4-72P, LOC100132830, 157 more genes
    nsv3922912copy number variation1nstd102humanPathogenic GRCh38 chr6: 90,687,494-93,806,515 , NCBI36 chr6: 91,453,934-94,572,954 , GRCh37 chr6: 91,397,213-94,516,233 LOC107986625, RN7SL415P, 18 more genes
    nsv3921478copy number variation1nstd102humanPathogenic NCBI36 chr6: 76,692,636-93,477,232 , GRCh38 chr6: 75,926,199-92,710,793 , GRCh37 chr6: 76,635,916-93,420,511 SPACA1, TAF13P1, 187 more genes
    nsv3919111copy number variation1nstd102humanPathogenic GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637 RNU6-770P, MAP3K5-AS2, 810 more genes
    nsv3918084copy number variation1nstd102humanPathogenic GRCh37 chr6: 86,513,991-93,898,976 , GRCh38 chr6: 85,804,273-93,189,258 , NCBI36 chr6: 86,570,710-93,955,697 LOC105377897, GABRR2, 91 more genes
    nsv3915765copy number variation1nstd102humanUncertain significance NCBI36 chr6: 91,425,377-94,604,519 , GRCh37.p13 chr6: 91,368,656-94,547,798 , GRCh38.p12 chr6: 90,658,937-93,838,080 LOC105377894, LINC02531, 18 more genes
    nsv3914309copy number variation1nstd102humanPathogenic GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194 ME1, GJB7, 136 more genes
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