ndst4[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3884707	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 115,928,747-115,940,452 , GRCh38.p12 chr4: 115,007,591-115,019,296	NDST4
nsv3881239	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 115,929,629-116,314,539 , GRCh38.p12 chr4: 115,008,473-115,393,383	NDST4, MRPS33P3
nsv3921840	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr4: 116,249,350-116,610,347 , GRCh37.p13 chr4: 116,029,901-116,390,898 , GRCh38.p12 chr4: 115,108,745-115,469,742	NDST4, MRPS33P3
nsv4728940	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 115,928,191-116,099,197 , GRCh38.p12 chr4: 115,007,035-115,178,041	NDST4, MRPS33P3
nsv4729325	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 115,844,816-116,266,652 , GRCh38.p12 chr4: 114,923,660-115,345,496	NDST4, MRPS33P3
nsv6290265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113	NDST4, LOC105379404, 218 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	NDST4, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	NDST4, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	NDST4, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	NDST4, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	NDST4, LOC105377343, 2341 more genes
nsv3875534	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 93,071,152-190,957,473 , GRCh38.p12 chr4: 92,150,001-190,036,318	NDST4, KLKB1, 1118 more genes
nsv6291432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354	NDST4, SNHG27, 1091 more genes
nsv3874596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 109,199,664-189,752,726 , GRCh38.p12 chr4: 108,278,508-188,831,572	NDST4, RPL6P12, 938 more genes
nsv6313878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443	NDST4, LINC00613, 448 more genes
nsv3920388	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207	NDST4, MIR576, 447 more genes
nsv3911834	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr4: 112,210,390-117,832,483 , GRCh37 chr4: 111,990,941-117,613,035 , GRCh38 chr4: 111,069,785-116,691,879	NDST4, ANK2, 71 more genes
nsv3885667	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 115,565,977-115,890,735 , GRCh38.p12 chr4: 114,644,821-114,969,579	NDST4, MIR577, 4 more genes
nsv3916316	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 111,318,515-191,263,063 , GRCh37.p13 chr4: 111,099,066-191,029,082 , GRCh38.p12 chr4: 110,177,910-190,107,927	NDST4, RNU7-194P, 939 more genes
nsv3872274	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 114,077,690-118,094,709 , GRCh37.p13 chr4: 113,858,241-117,875,261 , GRCh38.p12 chr4: 112,937,085-116,954,105	NDST4, LOC105377374, 39 more genes

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Items: 20

Number of Variants: 20

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