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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098787copy number variation1nstd102humanUncertain significance GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173 CUTA, SYNGAP1, 184 more genes
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv7040500inversion1nstd229human GRCh38 chr6: 33,421,287-33,425,725 , GRCh37.p13 chr6: 33,389,064-33,393,502 SYNGAP1
    nsv6570358inversion1nstd223human GRCh38 chr6: 32,570,902-37,403,160 , GRCh37.p13 chr6: 32,538,679-37,370,936 RN7SL273P, MKRN6P, 177 more genes
    nsv6565343inversion1nstd223human GRCh38 chr6: 32,527,987-37,402,848 , GRCh37.p13 chr6: 32,495,764-37,370,624 LOC105375022, SNRPC, 180 more genes
    nsv6562119inversion1nstd223human GRCh38 chr6: 32,527,628-37,403,016 , GRCh37.p13 chr6: 32,495,405-37,370,792 HLA-Z, ARMC12, 180 more genes
    nsv6556866inversion1nstd223human GRCh38 chr6: 32,527,208-37,403,016 , GRCh37.p13 chr6: 32,494,985-37,370,792 BAK1, HSD17B8, 180 more genes
    nsv6313582copy number variation1nstd102humanUncertain significance GRCh37 chr6: 33,069,892-33,751,391 , GRCh38.p12 chr6: 33,102,115-33,783,614 LOC107986537, MYL12BP3, 46 more genes
    nsv6312477copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 33,393,555-33,393,700 , GRCh38.p12 chr6: 33,425,778-33,425,923 SYNGAP1
    nsv6224148insertion1nstd214human GRCh38 chr6: 33,429,645-33,429,645 , GRCh37.p13 chr6: 33,397,422-33,397,422 SYNGAP1
    nsv6141387copy number variation1nstd206human GRCh38 chr6: 33,372,000-33,454,000 , GRCh37.p13 chr6: 33,339,777-33,421,777 KIFC1, PHF1, 6 more genes
    nsv6136501copy number variation1nstd213human GRCh37 chr6: 33,330,000-33,410,001 , GRCh38.p12 chr6: 33,362,223-33,442,224 KIFC1, PHF1, 6 more genes
    nsv6136500copy number variation1nstd213human GRCh37 chr6: 33,150,000-33,430,001 , GRCh38.p12 chr6: 33,182,223-33,462,224 COL11A2, RXRB, 30 more genes
    nsv6136154copy number variation1nstd213human GRCh37 chr6: 33,212,528-33,626,510 , GRCh38.p12 chr6: 33,244,751-33,658,733 BAK1, DAXX, 29 more genes
    nsv6135458copy number variation1nstd213human GRCh37 chr6: 33,212,528-33,626,510 , GRCh38.p12 chr6: 33,244,751-33,658,733 BAK1, DAXX, 29 more genes
    nsv5231786copy number variation1nstd204human GRCh38.p13 chr6: 33,016,601-33,499,100 , GRCh37.p13 chr6: 32,984,378-33,466,877 COL11A2, RXRB, 39 more genes
    nsv4940764copy number variation1nstd200human GRCh38 chr6: 33,443,728-33,443,906 , GRCh37.p13 chr6: 33,411,505-33,411,683 SYNGAP1
    nsv4768386copy number variation1nstd102humanLikely pathogenic GRCh38.p12 chr6: 33,375,382-33,468,170 , NCBI36 chr6: 33,451,137-33,543,925 , GRCh37.p13 chr6: 33,343,159-33,435,947 , GRCh37.p13 chr6|NT_167249.1: 4,836,050-4,916,187 , GRCh38.p12 chr6|NT_167249.2: 4,836,753-4,916,889 KIFC1, PHF1, 6 more genes
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