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Items: 1 to 20 of 154

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5902244copy number variation1nstd209human GRCh38 chr4: 156,014,074-164,864,480 , GRCh37.p13 chr4: 156,935,226-165,785,632 , MIR3688-1, 67 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5467009copy number variation1nstd206human GRCh38 chr4: 163,093,237-163,097,611 , GRCh37.p13 chr4: 164,014,389-164,018,763 MIR4454
    nsv5465293copy number variation1nstd206human GRCh38 chr4: 162,148,052-163,096,441 , GRCh37.p13 chr4: 163,069,204-164,017,593 LOC105377516, FSTL5, 3 more genes
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5039478inversion1nstd200human GRCh38 chr4: 158,116,539-168,149,530 , GRCh37.p13 chr4: 159,037,691-169,070,681 MIR4454, LOC105377520, 93 more genes
    nsv4948656copy number variation1nstd200human GRCh38 chr4: 161,988,485-163,518,479 , GRCh37.p13 chr4: 162,909,637-164,439,631 LOC105377517, MIR4454, 13 more genes
    nsv4936138copy number variation1nstd200human GRCh38 chr4: 163,084,022-163,096,111 , GRCh37.p13 chr4: 164,005,174-164,017,263 MIR4454
    nsv4875375inversion1nstd200human GRCh37 chr4: 163,506,313-164,180,082 , GRCh38.p12 chr4: 162,585,161-163,258,930 NAF1, MIR4454, 3 more genes
    nsv4801481copy number variation1nstd200human GRCh37 chr4: 164,014,382-164,018,734 , GRCh38.p12 chr4: 163,093,230-163,097,582 MIR4454
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
    nsv4457244copy number variation1nstd102humanPathogenic GRCh37 chr4: 151,174,061-190,957,473 , GRCh38.p12 chr4: 150,252,909-190,036,318 LOC105377509, MIR3140, 487 more genes
    nsv4455751copy number variation1nstd102humanUncertain significance GRCh37 chr4: 161,262,167-165,564,515 , GRCh38.p12 chr4: 160,341,015-164,643,363 YWHAQP4, NAF1, 25 more genes
    nsv4455301copy number variation1nstd102humanPathogenic GRCh37 chr4: 124,873,497-185,278,662 , GRCh38.p12 chr4: 123,952,342-184,357,509 SMARCA5, SFRP2, 633 more genes
    nsv4455294copy number variation1nstd102humanUncertain significance GRCh37 chr4: 162,592,951-164,285,653 , GRCh38.p12 chr4: 161,671,799-163,364,501 MTHFD2P4, NAF1, 10 more genes
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