snd1[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
nsv4675399	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 127,504,680-127,609,433 , GRCh38.p12 chr7: 127,864,627-127,969,380	SND1
nsv4456748	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 127,581,140-127,633,926 , GRCh38.p12 chr7: 127,941,087-127,993,873	SND1
nsv3887595	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 127,412,602-127,569,388 , GRCh38.p12 chr7: 127,772,548-127,929,335	SND1, LOC100196944
nsv3922595	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 127,313,125-127,444,243 , GRCh37.p13 chr7: 127,525,889-127,657,007 , GRCh38.p12 chr7: 127,885,836-128,016,954	SND1, SND1-IT1
nsv4456849	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 127,498,536-127,554,871 , GRCh38.p12 chr7: 127,858,483-127,914,818	SND1, LOC100196944
nsv4455645	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 127,461,295-127,504,681 , GRCh38.p12 chr7: 127,821,241-127,864,628	SND1, LOC100196944
nsv6314330	complex chromosomal rearrangement	7	nstd102	human	Likely pathogenic	GRCh37 chr2: 153,546,999-153,546,999 , GRCh37 chr2: 153,547,028-153,547,028 , GRCh37 chr5: 124,175,407-124,175,407 , GRCh37 chr5: 124,176,058-124,176,058 , GRCh37 chr5: 125,626,214-125,626,214 , GRCh37 chr5: 125,626,285-125,626,285 , GRCh37 chr6: 128,463,242-128,463,242 , GRCh37 chr6: 128,463,306-128,463,306 , GRCh37 chr6: 128,511,150-128,511,150 , GRCh37 chr6: 128,511,189-128,511,189 , GRCh37 chr6: 163,472,151-163,472,151 , GRCh37 chr6: 163,472,169-163,472,169 , GRCh37 chr7: 127,652,521-127,652,521 , GRCh37 chr7: 127,652,531-127,652,531 , GRCh38.p12 chr2: 152,690,485-152,690,485 , GRCh38.p12 chr2: 152,690,514-152,690,514 , GRCh38.p12 chr5: 124,839,714-124,839,714 , GRCh38.p12 chr5: 124,840,365-124,840,365 , GRCh38.p12 chr5: 126,290,522-126,290,522 , GRCh38.p12 chr5: 126,290,593-126,290,593 , GRCh38.p12 chr6: 128,142,097-128,142,097 , GRCh38.p12 chr6: 128,142,161-128,142,161 , GRCh38.p12 chr6: 128,190,005-128,190,005 , GRCh38.p12 chr6: 128,190,044-128,190,044 , GRCh38.p12 chr6: 163,051,119-163,051,119 , GRCh38.p12 chr6: 163,051,137-163,051,137 , GRCh38.p12 chr7: 128,012,468-128,012,468 , GRCh38.p12 chr6\|NT_187556.1: 539,378-539,378 , GRCh38.p12 chr6\|NT_187556.1: 491,431-491,431 , GRCh38.p12 chr7: 128,012,478-128,012,478 , GRCh38.p12 chr6\|NT_187556.1: 491,495-491,495 , GRCh38.p12 chr6\|NT_187556.1: 539,339-539,339	SND1, PTPRK, 3 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	SND1, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	SND1, LOC107986817, 2014 more genes
nsv3916726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440	SND1, LOC107986845, 245 more genes
nsv3900620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263	SND1, LSM8, 170 more genes
nsv3903275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 127,295,698-139,524,358 , GRCh38.p12 chr7: 127,655,644-139,824,559	SND1, RNU6-1272P, 224 more genes
nsv6313876	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839	SND1, IMPDH1, 174 more genes
nsv3910648	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 124,170,657-134,163,594 , GRCh37 chr7: 123,810,711-133,848,346 , NCBI36 chr7: 123,597,947-133,498,886	SND1, CPA1, 165 more genes
nsv6313722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 123,967,475-132,729,981 , GRCh38.p12 chr7: 124,327,421-133,045,221	SND1, IRF5, 153 more genes
nsv4455826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163	SND1, ASB15, 127 more genes
nsv3923164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016	SND1, GCC1, 104 more genes
nsv3915522	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 126,859,732-132,750,936 , NCBI36 chr7: 126,287,022-132,086,236 , GRCh37 chr7: 126,499,786-132,435,696	SND1, LRRC4, 126 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	SND1, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	SND1, RPL23AP51, 2684 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 37

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Number of Variants: 20

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