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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7039342inversion1nstd229human GRCh38 chr6: 86,041,090-92,871,248 , GRCh37.p13 chr6: 86,750,808-93,580,966 NDUFA5P9, AKIRIN2, 85 more genes
    nsv6817458copy number variation1nstd229human GRCh38 chr6: 88,095,728-88,140,532 , GRCh37.p13 chr6: 88,805,446-88,850,251 CNR1
    nsv6814648copy number variation1nstd229human GRCh38 chr6: 88,128,904-88,157,547 , GRCh37.p13 chr6: 88,838,623-88,867,266 CNR1
    nsv6813096copy number variation1nstd229human GRCh38 chr6: 88,102,245-88,163,688 , GRCh37.p13 chr6: 88,811,963-88,873,407 CNR1
    nsv6808584copy number variation1nstd229human GRCh38 chr6: 88,089,701-88,269,600 , GRCh37.p13 chr6: 88,799,419-88,979,319 RPS14P9, CNR1
    nsv6798856copy number variation1nstd229human GRCh38 chr6: 88,151,941-88,154,311 , GRCh37.p13 chr6: 88,861,660-88,864,030 CNR1
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631470copy number variation1nstd224human GRCh37 chr6: 88,843,390-88,867,925 , GRCh38.p12 chr6: 88,133,671-88,158,206 CNR1
    nsv6631469copy number variation2nstd224human GRCh37 chr6: 88,843,390-88,861,698 , GRCh38.p12 chr6: 88,133,671-88,151,979 CNR1
    nsv6631467copy number variation1nstd224human GRCh37 chr6: 88,817,786-88,861,698 , GRCh38.p12 chr6: 88,108,068-88,151,979 CNR1
    nsv6631340copy number variation1nstd224human GRCh37 chr6: 88,840,961-88,861,718 , GRCh38.p12 chr6: 88,131,242-88,151,999 CNR1
    nsv6571797inversion1nstd223human GRCh38 chr6: 88,146,222-88,147,178 , GRCh37.p13 chr6: 88,855,941-88,856,897 CNR1
    nsv6570894inversion1nstd223human GRCh38 chr6: 88,160,047-88,160,704 , GRCh37.p13 chr6: 88,869,766-88,870,423 CNR1
    nsv6408565copy number variation1nstd223human GRCh38 chr6: 88,128,904-88,157,547 , GRCh37.p13 chr6: 88,838,623-88,867,266 CNR1
    nsv6401692copy number variation1nstd223human GRCh38 chr6: 88,165,601-88,168,100 , GRCh37.p13 chr6: 88,875,320-88,877,819 CNR1
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6135938copy number variation1nstd213human GRCh37 chr6: 87,590,000-89,360,001 , GRCh38.p12 chr6: 86,880,282-88,650,282 ACTBP8, CGA, 33 more genes
    nsv6135855copy number variation1nstd213human GRCh37 chr6: 87,530,000-91,880,001 , GRCh38.p12 chr6: 86,820,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv6135527copy number variation1nstd213human GRCh37 chr6: 87,520,000-91,880,001 , GRCh38.p12 chr6: 86,810,282-91,170,283 ACTBP8, CGA, 67 more genes
    nsv5907523copy number variation1nstd209human GRCh38 chr6: 88,128,904-88,157,546 , GRCh37.p13 chr6: 88,838,623-88,867,265 CNR1
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