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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7147649copy number variation1nstd232human GRCh37.p13 chr17: 7,810,348-7,810,441 , GRCh38.p12 chr17: 7,907,030-7,907,123 CHD3
    nsv7095414copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936 CTC1, SAT2, 103 more genes
    nsv7095365copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310 TRK-TTT3-5, WRAP53, 59 more genes
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 MIR324, SLC2A4, 101 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv6989115copy number variation1nstd229human GRCh38 chr17: 7,900,907-8,010,227 , GRCh37.p13 chr17: 7,804,225-7,913,545 KCNAB3, RNF227, 5 more genes
    nsv6637360copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,381,537-8,068,400 , GRCh38.p12 chr17: 7,478,218-8,165,082 LOC107985075, TRT-AGT5-1, 53 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6314215copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,593,552-8,225,803 , GRCh38.p12 chr17: 7,690,234-8,322,485 GUCY2D, LOC105371520, 54 more genes
    nsv6314103copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972 RPL7AP64, TNK1, 87 more genes
    nsv6310334copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,135,555 , GRCh38.p12 chr17: 7,668,434-8,232,237 TRAPPC1, MIR4314, 51 more genes
    nsv6289425insertion1nstd214human GRCh38 chr17: 7,893,969-7,893,969 , GRCh37.p13 chr17: 7,797,287-7,797,287 CHD3
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 more genes
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv6129625insertion1nstd186human GRCh37 chr17: 7,788,663-7,788,676 , GRCh38.p12 chr17: 7,885,345-7,885,358 CHD3, NAA38
    nsv6090705insertion1nstd212human GRCh38 chr17: 7,885,307-7,885,307 , GRCh37.p13 chr17: 7,788,625-7,788,625 NAA38, CHD3
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